The NIH Toolbox for cognitive surveillance in Duchenne muscular dystrophy

OBJECTIVE: We performed a prospective, cross‐sectional cognitive assessment in subjects with Duchenne Muscular Dystrophy (DMD) and their biological mothers. METHODS: Thirty subjects with out‐of‐frame mutations in the dystrophin (DMD) gene, and 25 biological mothers were evaluated using the National...

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Detalles Bibliográficos
Autores principales: Thangarajh, Mathula, Kaat, Aaron J., Bibat, Genila, Mansour, Jennifer, Summerton, Katherine, Gioia, Anthony, Berger, Carly, Hardy, Kristina K., Wagner, Kathryn R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6764624/
https://www.ncbi.nlm.nih.gov/pubmed/31472009
http://dx.doi.org/10.1002/acn3.50867

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6764624/
https://www.ncbi.nlm.nih.gov/pubmed/31472009
http://dx.doi.org/10.1002/acn3.50867

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