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The Neurocognitive and Behavioral Profiles of 3 Brothers With Becker Muscular Dystrophy
Becker muscular dystrophy patients generally carry in-frame mutations in the dystrophin gene, allowing the production of partially functional dystrophin protein. The presence of cognitive and behavioral comorbidities and the relation with the location of mutations has been scarcely investigated in B...
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| Publié dans: | Child Neurol Open |
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| Auteurs principaux: | , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
SAGE Publications
2020
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7522818/ https://ncbi.nlm.nih.gov/pubmed/33029547 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/2329048X20957217 |
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