FRG2, an FSHD candidate gene, is transcriptionally upregulated in differentiating primary myoblast cultures of FSHD patients

Background: Autosomal dominant facioscapulohumeral muscular dystrophy (FSHD) is associated with partial deletion of the subtelomeric D4Z4 repeat array on chromosome 4qter. This chromosomal rearrangement may result in regional chromatin relaxation and transcriptional deregulation of genes nearby. Met...

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Detalhes bibliográficos
Main Authors: Rijkers, T, Deidda, G, van Koningsbrugge..., S, van Geel, M, Lemmers, R, van Deutekom, J C T, Figlewicz, D, Hewitt, J, Padberg, G, Frants, R, van der Maarel, S M
Formato: Artigo
Idioma:Inglês
Publicado em: BMJ Group 2004
Assuntos:
Original Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1735617/
https://ncbi.nlm.nih.gov/pubmed/15520407
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2004.019364
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