Phenotypes induced by NM causing α-skeletal muscle actin mutants in fibroblasts, Sol 8 myoblasts and myotubes

BACKGROUND: Nemaline myopathy is a neuromuscular disorder characterized by the presence of nemaline bodies in patient muscles. 20% of the cases are associated with α-skeletal muscle actin mutations. We previously showed that actin mutations can cause four different biochemical phenotypes and that ex...

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Detalles Bibliográficos
Autores principales: Vandamme, Drieke, Lambert, Ellen, Waterschoot, Davy, Tondeleir, Davina, Vandekerckhove, Joël, Machesky, Laura M, Constantin, Bruno, Rommelaere, Heidi, Ampe, Christophe
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Short Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2657152/
https://www.ncbi.nlm.nih.gov/pubmed/19284548
http://dx.doi.org/10.1186/1756-0500-2-40

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2657152/
https://www.ncbi.nlm.nih.gov/pubmed/19284548
http://dx.doi.org/10.1186/1756-0500-2-40

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