DUX4, a candidate gene of facioscapulohumeral muscular dystrophy, encodes a transcriptional activator of PITX1

Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal dominant disorder linked to contractions of the D4Z4 repeat array in the subtelomeric region of chromosome 4q. By comparing genome-wide gene expression data from muscle biopsies of patients with FSHD to those of 11 other neuromuscular dis...

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Détails bibliographiques
Auteurs principaux: Dixit, Manjusha, Ansseau, Eugénie, Tassin, Alexandra, Winokur, Sara, Shi, Rongye, Qian, Hong, Sauvage, Sébastien, Mattéotti, Christel, van Acker, Anne M., Leo, Oberdan, Figlewicz, Denise, Barro, Marietta, Laoudj-Chenivesse, Dalila, Belayew, Alexandra, Coppée, Frédérique, Chen, Yi-Wen
Format: Artigo
Langue:Inglês
Publié: National Academy of Sciences 2007
Sujets:
Biological Sciences
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC2084313/
https://ncbi.nlm.nih.gov/pubmed/17984056
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0708659104
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