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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...

詳細記述

保存先:
書誌詳細
出版年:Clin Transl Sci
主要な著者: Nalbandian, Angèle, Ghimbovschi, Svetlana, Wang, Zuyi, Knoblach, Susan, Llewellyn, Katrina J., Vesa, Jouni, Hoffman, Eric P., Kimonis, Virginia E.
フォーマット: Artigo
言語:Inglês
出版事項: John Wiley and Sons Inc. 2014
主題:
オンライン・アクセス: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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