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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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Dades bibliogràfiques
Publicat a:Ann Clin Transl Neurol
Autors principals: Thangarajh, Mathula, Kaat, Aaron J., Bibat, Genila, Mansour, Jennifer, Summerton, Katherine, Gioia, Anthony, Berger, Carly, Hardy, Kristina K., Wagner, Kathryn R.
Format: Artigo
Idioma:Inglês
Publicat: John Wiley and Sons Inc. 2019
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6764624/
https://ncbi.nlm.nih.gov/pubmed/31472009
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/acn3.50867
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