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...

Descripción completa

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

Internet

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

Ejemplares similares