New Insights into Genotype-phenotype Correlations in Chinese Facioscapulohumeral Muscular Dystrophy: A Retrospective Analysis of 178 Patients

BACKGROUND: Facioscapulohumeral muscular dystrophy (FSHD), a common autosomal dominant muscular disorder, is caused by contraction of the D4Z4 repeats on 4q35. The complicated genotype-phenotype correlation among different ethnic population remains a controversial subject. We aimed to refine this co...

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Detalles Bibliográficos
Autores principales: Lin, Feng, Wang, Zhi-Qiang, Lin, Min-Ting, Murong, Shen-Xing, Wang, Ning
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4733718/
https://www.ncbi.nlm.nih.gov/pubmed/26112708
http://dx.doi.org/10.4103/0366-6999.159336

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4733718/
https://www.ncbi.nlm.nih.gov/pubmed/26112708
http://dx.doi.org/10.4103/0366-6999.159336

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