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,...

Descripción completa

Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Study Protocol
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3852245/
https://www.ncbi.nlm.nih.gov/pubmed/24119284
http://dx.doi.org/10.1186/1471-2377-13-144

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3852245/
https://www.ncbi.nlm.nih.gov/pubmed/24119284
http://dx.doi.org/10.1186/1471-2377-13-144

Ejemplares similares