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Transgenic expression of inclusion body myopathy associated mutant p97/VCP causes weakness and ubiquitinated protein inclusions in mice.
Weihl CC, Miller SE, Hanson PI, Pestronk A. Weihl CC, et al. Among authors: pestronk a. Hum Mol Genet. 2007 Apr 15;16(8):919-28. doi: 10.1093/hmg/ddm037. Epub 2007 Feb 28. Hum Mol Genet. 2007. PMID: 17329348
Mutations in p97/VCP cause the autosomal-dominant, inherited syndrome inclusion body myopathy (IBM) associated with Paget's disease of the bone and frontotemporal dementia (IBMPFD) (Watts, G.D., Wymer, J., Kovach, M.J., Mehta, S.G., Mumm, S., Darvish, D., Pestronk, A …
Mutations in p97/VCP cause the autosomal-dominant, inherited syndrome inclusion body myopathy (IBM) associated with Paget's disease of the b …
317 results