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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Detalles Bibliográficos
Autores principales: Hellebrekers, Danique M. J., Vles, Johan S. H., Klinkenberg, Sylvia, Hendriksen, Jos G. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7522818/
https://www.ncbi.nlm.nih.gov/pubmed/33029547
http://dx.doi.org/10.1177/2329048X20957217

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7522818/
https://www.ncbi.nlm.nih.gov/pubmed/33029547
http://dx.doi.org/10.1177/2329048X20957217

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