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Global Gene Expression Profiling in R155H Knock‐In Murine Model of VCP Disease

Dominant mutations in the valosin‐containing protein (VCP) gene cause inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia, which is characterized by progressive muscle weakness, dysfunction in bone remodeling, and frontotemporal dementia. More recently, VCP has...

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Detalhes bibliográficos
Publicado no:Clin Transl Sci
Main Authors: Nalbandian, Angèle, Ghimbovschi, Svetlana, Wang, Zuyi, Knoblach, Susan, Llewellyn, Katrina J., Vesa, Jouni, Hoffman, Eric P., Kimonis, Virginia E.
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2014
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4329058/
https://ncbi.nlm.nih.gov/pubmed/25388089
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/cts.12241
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