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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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| Veröffentlicht in: | J Clin Neurol |
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| Hauptverfasser: | , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Korean Neurological Association
2015
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| Schlagworte: | |
| Online Zugang: | 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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