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Comparisons of intellectual capacities between mild and classic adult-onset phenotypes of myotonic dystrophy type 1 (DM1)

BACKGROUND: Myotonic dystrophy type 1 (DM1) is an autosomal dominant genetic multisystem disorder and the commonest adult-onset form of muscular dystrophy. DM1 results from the expansion of an unstable trinucleotide cytosine-thymine-guanine (CTG) repeat mutation. CTG repeats in DM1 patients can rang...

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Detalles Bibliográficos
Autores principales:	Jean, Stéphane, Richer, Louis, Laberge, Luc, Mathieu, Jean
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2014
Materias:	Research
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4247010/ https://www.ncbi.nlm.nih.gov/pubmed/25424323 http://dx.doi.org/10.1186/s13023-014-0186-5

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