DUX4 expression in FSHD muscle cells: how could such a rare protein cause a myopathy?

Facioscapulohumeral muscular dystrophy (FSHD) is one of the most frequent hereditary muscle disorders. It is linked to contractions of the D4Z4 repeat array in 4q35. We have characterized the double homeobox 4 (DUX4) gene in D4Z4 and its mRNA transcribed from the distal D4Z4 unit to a polyadenylatio...

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Bibliografiska uppgifter
Huvudupphovsmän: Tassin, Alexandra, Laoudj-Chenivesse, Dalila, Vanderplanck, Céline, Barro, Marietta, Charron, Sébastien, Ansseau, Eugénie, Chen, Yi-Wen, Mercier, Jacques, Coppée, Frédérique, Belayew, Alexandra
Materialtyp: Artigo
Språk:Inglês
Publicerad: Blackwell Publishing Ltd 2013
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Original Articles
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC3823138/
https://ncbi.nlm.nih.gov/pubmed/23206257
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1582-4934.2012.01647.x
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