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Myosin Storage Myopathy in C. elegans and Human Cultured Muscle Cells

Myosin storage myopathy is a protein aggregate myopathy associated with the characteristic subsarcolemmal accumulation of myosin heavy chain in muscle fibers. Despite similar histological findings, the clinical severity and age of onset are highly variable, ranging from no weakness to severe impairm...

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Detalles Bibliográficos
Autores principales: Dahl-Halvarsson, Martin, Pokrzywa, Malgorzata, Rauthan, Manish, Pilon, Marc, Tajsharghi, Homa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5268365/
https://www.ncbi.nlm.nih.gov/pubmed/28125727
http://dx.doi.org/10.1371/journal.pone.0170613