Comprehensive expression analysis of FSHD candidate genes at the mRNA and protein level

In facioscapulohumeral muscular dystrophy (FSHD) the majority of patients carry a D4Z4 macrosatellite repeat contraction in the subtelomere of chromosome 4q. Several disease mechanisms have been proposed to explain how repeat contraction causes muscular dystrophy. All proposed mechanisms foresee a c...

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Detaylı Bibliyografya
Asıl Yazarlar: Klooster, Rinse, Straasheijm, Kirsten, Shah, Bharati, Sowden, Janet, Frants, Rune, Thornton, Charles, Tawil, Rabi, van der Maarel, Silvère
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Nature Publishing Group 2009
Konular:
Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC2987013/
https://ncbi.nlm.nih.gov/pubmed/19809486
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2009.62
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