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Category:All HeadlinesWorld & GeopoliticsMarkets & EconomyTech & AIPoliticsSearch results for: "Systematic genotype–pheno" (30 stories)

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Systematic genotype–phenotype mapping and transcriptomic analyses highlight SEMA6A as a candidate for neuronal migration defects in 5q22–q23 deletions
Lead StoryNaturegeneral
Aug 27

Systematic genotype–phenotype mapping and transcriptomic analyses highlight SEMA6A as a candidate for neuronal migration defects in 5q22–q23 deletions

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE04ZURRc3ZRak1WbjZqdUlKYnlGTFRjRHB2bnpWbjZhS3oxa3FsQVlWV2doUWJuNWJYY2xLOF92Q1ZiN0FiZGFiTlh5Vkt6bVZsTFZ6Z2ZHS2psMkdGdEc0?oc=5" target="_blank">Systematic genotype–phenotype mapping and transcriptomic analyses highlight SEMA6A as a candidate for neuronal migration defects in 5q22–q23 deletions</a>  <font color="#6f6f6f">Nature</font>

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Search Results for "Systematic genotype–pheno"

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29 stories displayed
Dynamic phenotype monitoring to prevent genotype–phenotype discrepancies in pharmacogenetic-guided drug therapy
Frontiersgeneral

Dynamic phenotype monitoring to prevent genotype–phenotype discrepancies in pharmacogenetic-guided drug therapy

<a href="https://news.google.com/rss/articles/CBMilAFBVV95cUxPN3lnMTdJS3RZaUdwSmVJQ0xLVmpRdFgxNFRBbU5tdEJ4VVNIdHdhekRRdllyOWozQ0llZWJiTVNIMnZfb25kVUdsY3JZTDhTTm9kbWItc1VHTUR5NnBvbUg5N3VNYmx3TVh0Z0tRdldQSVBjejBOdHB2d0JyMVFpMEpEdGFrNUJhcHI1cWVPZDJ4aFRa?oc=5" target="_blank">Dynamic phenotype monitoring to prevent genotype–phenotype discrepancies in pharmacogenetic-guided drug therapy</a>  <font color="#6f6f6f">Frontiers</font>

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PURA-Related Neurodevelopmental Disorder: A Comprehensive Clinical Review of Genetics, Phenotype, and Emerging Therapeutic Strategies
Cureusgeneral

PURA-Related Neurodevelopmental Disorder: A Comprehensive Clinical Review of Genetics, Phenotype, and Emerging Therapeutic Strategies

<a href="https://news.google.com/rss/articles/CBMi_gFBVV95cUxOQ2ZrYkN5YnI2RVYyd2NhNGdGTFJNRF82RnNRd0l1TDhxWTFGOS1iQ0pNclc4akFvazlQYXdCMEI0ZnQ2WjZCclNIbVl2elNXdVZLOGk3aTBlalRweU55eW0yX0dSOC1BdE93NTZHOVdvZnV3OEo3Y1lod3V1VDFCa1lERmNpOGtPdUxXN09ORVk4UzV6WnRBMmtzT0NmLVV6cmMzMGZDdTRETVZ2M1JXYUk0MVJPUldSYnpnMEFNUW5GYUFMekV0ckFIalc2Tzd3VmdRbHNpZDdXdS12SEZ3QTJVTDNJUXhUS2s1eUJYcGNuMDZlSTltOEJSdzRuQQ?oc=5" target="_blank">PURA-Related Neurodevelopmental Disorder: A Comprehensive Clinical Review of Genetics, Phenotype, and Emerging Therapeutic Strategies</a>  <font color="#6f6f6f">Cureus</font>

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Systematic reassessment of reported variants in individuals with suspicion of Alport spectrum disorder reveals a high rate of ambiguous results
Naturegeneral

Systematic reassessment of reported variants in individuals with suspicion of Alport spectrum disorder reveals a high rate of ambiguous results

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE9hNlZRbnBZTUdfdzBSREI0a3BWT3Y0T3V4LWVibl8yUlhObGw0WjhOZEZTUnNjdzg4RUxadEpFSGdyTUpackRTNnhoRUZkOTJQdVREN01mR2dfUkRPZ1Rz?oc=5" target="_blank">Systematic reassessment of reported variants in individuals with suspicion of Alport spectrum disorder reveals a high rate of ambiguous results</a>  <font color="#6f6f6f">Nature</font>

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Genotype‐phenotype analysis of selective failure of tooth eruption—A systematic review
Wiley Online Librarytech

Genotype‐phenotype analysis of selective failure of tooth eruption—A systematic review

<a href="https://news.google.com/rss/articles/CBMiakFVX3lxTFBXWkRvM3VTblB5R3I2T0pwYThlYkhnWDF5VFFnREl1OFM3S0RsZERxdEVDVjBjMWNJemtaVmdTZmpXbzI4WElHWUlhVEI4QWg2WFlUR3F3aWVOY1hEcGRxd1pqYXE2OW9wb0E?oc=5" target="_blank">Genotype‐phenotype analysis of selective failure of tooth eruption—A systematic review</a>  <font color="#6f6f6f">Wiley Online Library</font>

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Large-Scale Genotype-Phenotype Landscape Measurements for Precision Engineering of Living Measurement Systems
National Institute of Standards and Technology (.gov)general

Large-Scale Genotype-Phenotype Landscape Measurements for Precision Engineering of Living Measurement Systems

<a href="https://news.google.com/rss/articles/CBMivgFBVV95cUxQc3RySmtieXVYcmRpSG5xQnN3S0JEZ2xXckVNT2JLc0U5Q3U4aER5dkk5VnktRnBaNFVsbFphQ1NjR29yMDZHY2JTZU9hUVVYaUxxVnpYS2k4djhVZjNNWWo3NFNtNmxmQzhzUlNiOGlJTmVEOGZwTmpOT0FTNTFvbGFMSHl3ekQyVHhjZld6d1J4bTRJMWIzNWI4MlVlVTZjclljUzRZQ3dHbDVhTUJmemx5N3JpM0xKc3RIcjZB?oc=5" target="_blank">Large-Scale Genotype-Phenotype Landscape Measurements for Precision Engineering of Living Measurement Systems</a>  <font color="#6f6f6f">National Institute of Standards and Technology (.gov)</font>

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Deep mutational scanning: A versatile tool in systematically mapping genotypes to phenotypes
Frontiersgeneral

Deep mutational scanning: A versatile tool in systematically mapping genotypes to phenotypes

<a href="https://news.google.com/rss/articles/CBMijwFBVV95cUxNaGY4a1FFQWd2RzRnUlZJa2xib2ozVHBSTGViZnpRdUlOV3kwM25qRlNqdGlmR1hSb0hZclFaVEhrQTlfcGw3YnhFVkYzQVIyTGxWcG1ySW0yWG9zd0Y2Y0VRQ1o0bWtlejRxUEZhNW5WMFg2TWhqTGNXSlBkRElDanpNTW5DQVdCMXAzYzNsSQ?oc=5" target="_blank">Deep mutational scanning: A versatile tool in systematically mapping genotypes to phenotypes</a>  <font color="#6f6f6f">Frontiers</font>

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Genotype–phenotype correlations in WHIM syndrome: a systematic characterization of CXCR4
Naturegeneral

Genotype–phenotype correlations in WHIM syndrome: a systematic characterization of CXCR4

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTFBmZHVZaXYya2FLd01CSDlJdFlsN1dYZ2JiOEdSejczMG9GTURBX05rSnlJUERqb3E2UDJGOXFZWURwTWp4TUgyT2Q1MjN4Nzg4OHpTdkRyWVgzamllMm1Z?oc=5" target="_blank">Genotype–phenotype correlations in WHIM syndrome: a systematic characterization of CXCR4</a>  <font color="#6f6f6f">Nature</font>

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Case report: p.Glu134del SOD1 mutation in two apparently unrelated ALS patients with mirrored phenotype
Frontiersworld

Case report: p.Glu134del SOD1 mutation in two apparently unrelated ALS patients with mirrored phenotype

<a href="https://news.google.com/rss/articles/CBMikAFBVV95cUxOaEQwRTdmQTRkNDZWV3ZvXzdVSnpKb2JoSU5KQThCeFFuM2FsU2oxeW1fTEpPdXpqbVhlY2NyQWhRamdKQ0RGMUo2Tm1GZ2RadnVBWTAydTlkb0kzZWVmODZJekdhMW56Y055NFo1TjZtbTBQZEhhLXZVYjlCZ2lTT3drazVCWWVSM0p6eWhyYXA?oc=5" target="_blank">Case report: p.Glu134del SOD1 mutation in two apparently unrelated ALS patients with mirrored phenotype</a>  <font color="#6f6f6f">Frontiers</font>

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Examining genotype-phenotype associations of GRAM domain proteins using GWAS, PheWAS and literature review in cattle, human, pig, mouse and chicken
Naturetech

Examining genotype-phenotype associations of GRAM domain proteins using GWAS, PheWAS and literature review in cattle, human, pig, mouse and chicken

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE03elZiWDhRSTF6LV9zTmpLN1NfazZFeWFGSklnR2lqa0lLZEMzdjFDazBqbXJqWWNTUmMtcnZOcldDMzlTLWt1a1FNNnZSTk51LWFzSzBtT05HYmd4OGtj?oc=5" target="_blank">Examining genotype-phenotype associations of GRAM domain proteins using GWAS, PheWAS and literature review in cattle, human, pig, mouse and chicken</a>  <font color="#6f6f6f">Nature</font>

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Advances in PMP22 sequence variant-associated hereditary neuropathy with liability to pressure palsies: from gene dosage effects to mechanism-informed variant interpretation
Frontiersgeneral

Advances in PMP22 sequence variant-associated hereditary neuropathy with liability to pressure palsies: from gene dosage effects to mechanism-informed variant interpretation

<a href="https://news.google.com/rss/articles/CBMikAFBVV95cUxPUzh0bXVLVEhpM2FZLWJ5dzVycllhMUVWWFZOSHRHaWw0QTNhcG41NEEtYmZIVi0yTWZwcEMzdXNMaTFydC13RkdscV81czRwaUk2R3ZFV1BRNVItVG1ya1lfSGl2VHg0Z2NFLTlzZWt2cW92eUpyV3RVNzVKZmhKbkFQMkhRZHpzRmdIQ3RDWE0?oc=5" target="_blank">Advances in PMP22 sequence variant-associated hereditary neuropathy with liability to pressure palsies: from gene dosage effects to mechanism-informed variant interpretation</a>  <font color="#6f6f6f">Frontiers</font>

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A single-cell resolved genotype-phenotype map using genome-wide genetic and environmental perturbations
Naturegeneral

A single-cell resolved genotype-phenotype map using genome-wide genetic and environmental perturbations

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE5walZhMUpwdkY4WnVvR1pYWXhzZEhZbFlXVXUxcEI2cUxxODFGYmtPb3ZsczV5LS1Va1lVRjhRSWVRRGU0Q0tCb0J3bTBHak1uWVlYUHdBak0xZ2hQWmNV?oc=5" target="_blank">A single-cell resolved genotype-phenotype map using genome-wide genetic and environmental perturbations</a>  <font color="#6f6f6f">Nature</font>

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A systematic review and meta-analysis of GFAP gene variants in Alexander disease
Naturegeneral

A systematic review and meta-analysis of GFAP gene variants in Alexander disease

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE9wemRyU0VnUHhqS1lka1RfWWxwVExIOFpVZTVOQ0FNQ2R3LU5WRVhiSFk0NlpVTDZhb05nNDdLOFYySTNnaUJSTVI5TDdkYTBUNTdCaTRyMU9sUXBmLWpv?oc=5" target="_blank">A systematic review and meta-analysis of GFAP gene variants in Alexander disease</a>  <font color="#6f6f6f">Nature</font>

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Identification of genetic variants associated with lupus nephritis in a Taiwanese cohort through systematic genetic screening
Naturetech

Identification of genetic variants associated with lupus nephritis in a Taiwanese cohort through systematic genetic screening

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE1fOHFQWHFfMEp2ZVNwcUZ6R2lPa0haT2ZyNTJOQWQ2TVRIOVIzMkJNbnU4SGdQLTk5Ry1GV2lEa3JVTzkyMDJhR0Rtd2N6Tm1lUTNlRmVQNmhnN0EtYi04?oc=5" target="_blank">Identification of genetic variants associated with lupus nephritis in a Taiwanese cohort through systematic genetic screening</a>  <font color="#6f6f6f">Nature</font>

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Genotype-phenotype relationship in patients with arrhythmogenic right ventricular cardiomyopathy caused by desmosomal gene mutations: A systematic review and meta-analysis
Naturegeneral

Genotype-phenotype relationship in patients with arrhythmogenic right ventricular cardiomyopathy caused by desmosomal gene mutations: A systematic review and meta-analysis

<a href="https://news.google.com/rss/articles/CBMiU0FVX3lxTFBubUJDcDE5LVhSNHRRc1VqcHdaR1hrRXdmc1FlVFZaYXptRFNsNnpET1dhYklPQ3NOa0pkeXBGVHNmbEtXekJIUkdFSGctTDVGOXY0?oc=5" target="_blank">Genotype-phenotype relationship in patients with arrhythmogenic right ventricular cardiomyopathy caused by desmosomal gene mutations: A systematic review and meta-analysis</a>  <font color="#6f6f6f">Nature</font>

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Systematic characterization of gene function in the photosynthetic alga Chlamydomonas reinhardtii
Natureworld

Systematic characterization of gene function in the photosynthetic alga Chlamydomonas reinhardtii

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE1zU0Znd256NlpSeVdSYmRIdEZuOFpld1Bya0Z2SmlRNlBSLWdWZXNlY21OTURoZklhNDJDZkl4V0dNbFVGQkMzSDdsSUpNZzlmd2xTNFZKa0kxZXZzczZJ?oc=5" target="_blank">Systematic characterization of gene function in the photosynthetic alga Chlamydomonas reinhardtii</a>  <font color="#6f6f6f">Nature</font>

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The phenotypic spectrum and genotype-phenotype correlations in 106 patients with variants in major autism gene CHD8
Naturegeneral

The phenotypic spectrum and genotype-phenotype correlations in 106 patients with variants in major autism gene CHD8

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE5VSTIyekZCLVItSDZlTUVVeUdXazRpcDNuaUNCNHBOTUZtVFM0Nk5BRXk5SFE2bDFpSzFoakVyNW9HZ2trckQwWXNodzFJc3otTFhjTlNyUmdmdThQMVBj?oc=5" target="_blank">The phenotypic spectrum and genotype-phenotype correlations in 106 patients with variants in major autism gene CHD8</a>  <font color="#6f6f6f">Nature</font>

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Systematic discovery of gene-environment interactions underlying the human plasma proteome in UK Biobank
Naturemarkets

Systematic discovery of gene-environment interactions underlying the human plasma proteome in UK Biobank

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTFB0U0ZWMlRtanNMX0Rjd2xlR3pzZm1TS3pxTDBTS0JpVU5RZ3kwSUVzSmpjZ2VoVDR6c3I5NVBVZWM4OXdSX2sxR01FZ0pZN0loaGdKbHdmOVRYN3pZQ1Jz?oc=5" target="_blank">Systematic discovery of gene-environment interactions underlying the human plasma proteome in UK Biobank</a>  <font color="#6f6f6f">Nature</font>

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ZMYND11 p.Arg600Trp variant associated with a distinctive neurodevelopmental phenotype
Naturegeneral

ZMYND11 p.Arg600Trp variant associated with a distinctive neurodevelopmental phenotype

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE40T3VwZzNYM0UxOVNzd185R2NycnpIRnA5NHZiQ1RLa29wejQtMFpjQWV0Q0NGenVwSmVqdjJUU3dPcnVPZHVtUFdNNW96bV9IUEY2dURfSDVHdGh1d0Rz?oc=5" target="_blank">ZMYND11 p.Arg600Trp variant associated with a distinctive neurodevelopmental phenotype</a>  <font color="#6f6f6f">Nature</font>

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Genetic polymorphisms associated with obesity in the Arab world: a systematic review
Natureworld

Genetic polymorphisms associated with obesity in the Arab world: a systematic review

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTFBMZEVfdzVxNko4a0dYakVBN0lBUUpGYXNRR2ljX0FRd3ctN0NhSnNQR1c5bVpsQlB6clhBZW9vMXlxOFBDemJKQklUTjZ3d2NNRUxESl9pOWNpTGNfaVk0?oc=5" target="_blank">Genetic polymorphisms associated with obesity in the Arab world: a systematic review</a>  <font color="#6f6f6f">Nature</font>

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Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers
Naturetech

Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE5kVUlyZlpKVUxmcVVkYzR0UXRWdnZYVkl4bUc3cURqTmVzWkluNk5GWHV0em1WX0VwSEdXQ2N1RF9nOG5JWDFNOGotRmlncHdKMEhJYVgtZFJrSmlZSlRJ?oc=5" target="_blank">Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers</a>  <font color="#6f6f6f">Nature</font>

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Treatment of mucopolysaccharidosis type II (Hunter syndrome): results from a systematic evidence review
Natureworld

Treatment of mucopolysaccharidosis type II (Hunter syndrome): results from a systematic evidence review

<a href="https://news.google.com/rss/articles/CBMiU0FVX3lxTE5Uc3VDMnV3UzZWak9HT1hWbmhEc3FkZzJBTDctc2JvYVUtVnZsclJWMGViTW80WTdpZ3owY3VHaU1mTWhrTXV2b3Z3NkNtWDF0VWRZ?oc=5" target="_blank">Treatment of mucopolysaccharidosis type II (Hunter syndrome): results from a systematic evidence review</a>  <font color="#6f6f6f">Nature</font>

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The congenital hearing phenotype in GJB2 in Queensland, Australia: V37I and mild hearing loss predominates
Naturegeneral

The congenital hearing phenotype in GJB2 in Queensland, Australia: V37I and mild hearing loss predominates

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE1DS1ZLN0N5VHI4cGxEc1ZEaTdpYXBveFFlRUZpelMwb3FLNkZaRkJQWEd2RFhuVlJLb294NWlSQXBEZDhsUnR5NHA1QVhCWmFhRFI0UXJUNnZYbWNQQ0Jj?oc=5" target="_blank">The congenital hearing phenotype in GJB2 in Queensland, Australia: V37I and mild hearing loss predominates</a>  <font color="#6f6f6f">Nature</font>

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Evaluating the quality of Marfan genotype–phenotype correlations in existing FBN1 databases
Naturegeneral

Evaluating the quality of Marfan genotype–phenotype correlations in existing FBN1 databases

<a href="https://news.google.com/rss/articles/CBMiVEFVX3lxTE9PV1JUdFJUcEEzNUFPNVdfRXpoM1pWTEVSbUNJVVlhVl9KcGk5eWx1eDUzUEp4bUJrdzJZTlFBVkYtNzJHeEs4VWx3Q1lfaFBoUjZ4NQ?oc=5" target="_blank">Evaluating the quality of Marfan genotype–phenotype correlations in existing FBN1 databases</a>  <font color="#6f6f6f">Nature</font>

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Craniofacial syndromes and class III phenotype: common genotype fingerprints? A scoping review and meta-analysis
Naturegeneral

Craniofacial syndromes and class III phenotype: common genotype fingerprints? A scoping review and meta-analysis

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE5pLWJ0S1pKQW9ncFRGM0JxcGtMYlZ0SUVXSElMQVJxRVNiUWo1b1kxYzg3SHpZVXFjdkU0RzdzZkw5VTdmWDctemE3Nm5OV2NiSjUzd0JyUjRZMEUwNGkw?oc=5" target="_blank">Craniofacial syndromes and class III phenotype: common genotype fingerprints? A scoping review and meta-analysis</a>  <font color="#6f6f6f">Nature</font>

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Clinical relevance of systematic phenotyping and exome sequencing in patients with short stature
Naturegeneral

Clinical relevance of systematic phenotyping and exome sequencing in patients with short stature

<a href="https://news.google.com/rss/articles/CBMiVEFVX3lxTE1vVE4xS19BeTJ5b0NaWUc0SF80dVNwdkhTVnVVdy1Vci13UUtYNVVGTVNacG9MZnJDeS0xU3dlWEFURzVsRW1FOHpKRzJUSnNJd2U3NQ?oc=5" target="_blank">Clinical relevance of systematic phenotyping and exome sequencing in patients with short stature</a>  <font color="#6f6f6f">Nature</font>

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CRISPR Technology Maps Every Human Gene Function
Genetic Engineering and Biotechnology Newstech

CRISPR Technology Maps Every Human Gene Function

<a href="https://news.google.com/rss/articles/CBMikwFBVV95cUxNNkN1Vk5KVEpFb2hnQmZYemtMa3pHRHF2d0FXMkhoYlUyazNaS1ZURV96ek1zdnFJenNOTkdSSndobDhieWV5YzVZcGdFTlhfcmVDQ19Rb2ZKVFMzd1NQV3pUUUczaHgzVEFEVWlUS2VRQXNHNGYwVV9IWjF3T212cVNORFFodFNvMi13Q2d3QmZ5WGs?oc=5" target="_blank">CRISPR Technology Maps Every Human Gene Function</a>  <font color="#6f6f6f">Genetic Engineering and Biotechnology News</font>

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Updated MDSGene review on the clinical and genetic spectrum of LRRK2 variants in Parkinson´s disease
Naturegeneral

Updated MDSGene review on the clinical and genetic spectrum of LRRK2 variants in Parkinson´s disease

<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTFBoZEItRVIxMU5XVGlsc0stSGhkT0Z0RGxmdTdWekhMVkdXZlotTTdTRk5hNEpWLXhHdUpxVVVSdXJHbm5ReXR3R3Uzd3I5RUVPNWY4TGFFY3FENnRaN3BF?oc=5" target="_blank">Updated MDSGene review on the clinical and genetic spectrum of LRRK2 variants in Parkinson´s disease</a>  <font color="#6f6f6f">Nature</font>

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Genotype-phenotype correlations in hereditary hemorrhagic telangiectasia: Data from the French-Italian HHT network
Naturegeneral

Genotype-phenotype correlations in hereditary hemorrhagic telangiectasia: Data from the French-Italian HHT network

<a href="https://news.google.com/rss/articles/CBMiUkFVX3lxTE1vNGJIbjJBRzBoSWFfUUhYaHlydlI4YTVIVWFZaHp4TXpCRUowWm5EZXlBNlFyazV2Y2NCYzAyUUJBOWJYNFhUU3FtbUtaMEw0N3c?oc=5" target="_blank">Genotype-phenotype correlations in hereditary hemorrhagic telangiectasia: Data from the French-Italian HHT network</a>  <font color="#6f6f6f">Nature</font>

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DMD deletions underlining mild dystrophinopathies: literature review highlights phenotype-related mutation clusters and provides insights about genetic mechanisms and prognosis
Frontiersworld

DMD deletions underlining mild dystrophinopathies: literature review highlights phenotype-related mutation clusters and provides insights about genetic mechanisms and prognosis

<a href="https://news.google.com/rss/articles/CBMikAFBVV95cUxPWXFNUUQxb3owb0NHUng5Q0lVUDhEQWF0X0tTM1BPQnZ6eG9tU2laQmQ1YVdESmV4QVpWeE5oM3NjbE1mTlJ2NHBWWmZ3YjFqcFozeFJHTmhNazU0VjRqbEZ3Z1YtNUw0NVlGOWhMOHZOcjFLSGNwbmRRNk90V0I1TFMtZkxMdmp4V1JxSy1UUmo?oc=5" target="_blank">DMD deletions underlining mild dystrophinopathies: literature review highlights phenotype-related mutation clusters and provides insights about genetic mechanisms and prognosis</a>  <font color="#6f6f6f">Frontiers</font>

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