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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Detalles Bibliográficos
Publicado en: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: John Wiley and Sons Inc. 2014
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Original Research Articles
Acceso en liña: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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