Determining the role of sarcomeric proteins in facioscapulohumeral muscular dystrophy: a study protocol

BACKGROUND: Although muscle weakness is a hallmark of facioscapulohumeral muscular dystrophy (FSHD), the molecular mechanisms that lead to weakness in FSHD remain largely unknown. Recent studies suggest aberrant expression of genes involved in skeletal muscle development and sarcomere contractility,...

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Detaylı Bibliyografya
Asıl Yazarlar: Lassche, Saskia, Ottenheijm, Coen AC, Voermans, Nicol C, Westeneng, Henk-Jan, Janssen, Barbara H, van der Maarel, Silvère M, Hopman, Maria T, Padberg, George W, Stienen, Ger JM, van Engelen, Baziel GM
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BioMed Central 2013
Konular:
Study Protocol
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3852245/
https://ncbi.nlm.nih.gov/pubmed/24119284
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2377-13-144
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