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A family history of DUX4: phylogenetic analysis of DUXA, B, C and Duxbl reveals the ancestral DUX gene

BACKGROUND: DUX4 is causally involved in the molecular pathogenesis of the neuromuscular disorder facioscapulohumeral muscular dystrophy (FSHD). It has previously been proposed to have arisen by retrotransposition of DUXC, one of four known intron-containing DUX genes. Here, we investigate the evolu...

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Detaylı Bibliyografya
Asıl Yazarlar: Leidenroth, Andreas, Hewitt, Jane E
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BioMed Central 2010
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3004920/
https://ncbi.nlm.nih.gov/pubmed/21110847
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2148-10-364
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