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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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| Publicat a: | J Clin Neurol |
|---|---|
| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Korean Neurological Association
2015
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4507379/ https://ncbi.nlm.nih.gov/pubmed/26022459 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3988/jcn.2015.11.3.248 |
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