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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Detalles Bibliográficos
Main Authors: 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
Formato: Artigo
Idioma:Inglês
Publicado: BioMed Central 2013
Assuntos:
Study Protocol
Acceso en liña: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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