Function and Structure ofVCPMutations Leading to Inclusion-Body Myopathy Associated with Paget Disease of Bone and Frontotemporal Dementia-Reference-Cited by-同舟云学术

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Function and Structure ofVCPMutations Leading to Inclusion-Body Myopathy Associated with Paget Disease of Bone and Frontotemporal Dementia

Published:2011-12-19 Issue: Volume: Page:206-218
ISSN:
Container-title:Muscle Aging, Inclusion-Body Myositis and Myopathies
language:
Short-container-title:

Author:

Wójcik Cezary

Publisher

Wiley-Blackwell

Reference148 articles.

1. Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein;Watts;Nat Genet,2004

2. Inclusion body myopathy-associated mutations in p97/VCP impair endoplasmic reticulum-associated degradation;Weihl;Hum Mol Genet,2006

3. Mutant valosin-containing protein causes a novel type of frontotemporal dementia;Schroder;Ann Neurol,2005

4. Novel ubiquitin neuropathology in frontotemporal dementia with valosin-containing protein gene mutations;Forman;J Neuropathol Exp Neurol,2006

5. Autosomal dominant inclusion body myopathy, Paget disease of bone, and frontotemporal dementia;Kimonis;Alzheimer Dis Assoc Disord,2005

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