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Valosin containing protein associated inclusion body myopathy: abnormal vacuolization, autophagy and cell fusion in myoblasts

Inclusion body myopathy associated with Paget’s disease and frontotemporal dementia (IBMPFD) is caused by mutations in the valosin containing protein (VCP) gene. The disease is associated with progressive proximal muscle weakness, inclusions and vacuoles in muscle fibers, malfunction in the bone rem...

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Bibliografski detalji
Glavni autori: Vesa, Jouni, Su, Hailing, Watts, Giles D., Krause, Sabine, Walter, Maggie C., Wallace, Douglas C., Kimonis, Virginia E.
Format: Artigo
Jezik:Inglês
Izdano: 2009
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC2782446/
https://ncbi.nlm.nih.gov/pubmed/19828315
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nmd.2009.08.003
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