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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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| Publicado no: | Clin Transl Sci |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2014
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| 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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