Author:
Llewellyn Katrina J.,Nalbandian Angèle,Weiss Lan N.,Chang Isabela,Yu Howard,Khatib Bibo,Tan Baichang,Scarfone Vanessa,Kimonis Virginia E.
Funder
UC Irvine Institute of Clinical Translational Science (ICTS)
California Stem Cell Clinical Fellowship
NIAMS, National Institute of Health, R01 and R56
Publisher
Public Library of Science (PLoS)
Reference98 articles.
1. Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein;GD Watts;Nature Genet,2004
2. Autosomal dominant inclusion body myopathy, Paget disease of bone, and frontotemporal dementia;VE Kimonis;Alzheimer disease and associated disorders,2005
3. Clinical and molecular studies in a unique family with autosomal dominant limb-girdle muscular dystrophy and Paget disease of bone;VE Kimonis;Genet Med,2000
4. VCP disease associated with myopathy, Paget disease of bone and frontotemporal dementia: review of a unique disorder;VE Kimonis;Biochimica et Biophysica Acta,2008
5. The multiple faces of valosin-containing protein-associated diseases: inclusion body myopathy with Paget's disease of bone, frontotemporal dementia, and amyotrophic lateral sclerosis;A Nalbandian;J Mol Neurosci,2011
Cited by
10 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献