Clinical and Genetic Characterization of Female Dystrophinopathy

BACKGROUND AND PURPOSE: Duchenne and Becker muscular dystrophies are the most common X-linked recessive muscular dystrophies. Dystrophin gene mutations usually affect men, but reportedly 2.5-7.8% of women are affected and are classified as symptomatic carriers. The aim of this study was to clinicall...

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Detalles Bibliográficos
Autores principales: Lee, Seung Ha, Lee, Jung Hwan, Lee, Kyung-A, Choi, Young-Chul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Neurological Association 2015
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4507379/
https://www.ncbi.nlm.nih.gov/pubmed/26022459
http://dx.doi.org/10.3988/jcn.2015.11.3.248

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4507379/
https://www.ncbi.nlm.nih.gov/pubmed/26022459
http://dx.doi.org/10.3988/jcn.2015.11.3.248

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