Profound misregulation of muscle-specific gene expression in facioscapulohumeral muscular dystrophy

Facioscapulohumeral muscular dystrophy (FSHD) is a neuromuscular disorder characterized by an insidious onset and progressive course. The disease has a frequency of about 1 in 20,000 and is transmitted in an autosomal dominant fashion with almost complete penetrance. Deletion of an integral number o...

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Detalles Bibliográficos

Publicado en:	Proc Natl Acad Sci U S A
Principais autores:	Tupler, Rossella, Perini, Giovanni, Pellegrino, Maria Antonietta, Green, Michael R.
Formato:	Artigo
Idioma:	Inglês
Publicado:	National Academy of Sciences 1999
Assuntos:	Biological Sciences
Acceso en liña:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC23032/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/10535977/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.96.22.12650
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