Myoblasts from affected and non-affected FSHD muscles exhibit morphological differentiation defects

Facioscapulohumeral dystrophy (FSHD) is a muscular hereditary disease with a prevalence of 1 in 20,000 caused by a partial deletion of a subtelomeric repeat array on chromosome 4q. However, very little is known about the pathogenesis as well as the molecular and biochemical changes linked to the pro...

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Detalles Bibliográficos
Autores principales: Barro, Marietta, Carnac, Gilles, Flavier, Sébastien, Mercier, Jacques, Vassetzky, Yegor, Laoudj-Chenivesse, Dalila
Formato: Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2010
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2910739/
https://www.ncbi.nlm.nih.gov/pubmed/18505476
http://dx.doi.org/10.1111/j.1582-4934.2008.00368.x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2910739/
https://www.ncbi.nlm.nih.gov/pubmed/18505476
http://dx.doi.org/10.1111/j.1582-4934.2008.00368.x

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