Valosin-containing protein disease: Inclusion body myopathy with Paget’s disease of the bone and fronto-temporal dementia
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health
Reference88 articles.
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2. Autosomal dominant inclusion body myopathy, Paget disease of bone, and frontotemporal dementia;Kimonis;Alzheimer Dis Assoc Disord,2005
3. Valosin-containing protein gene mutations: clinical and neuropathologic features;Guyant-Marechal;Neurology,2006
4. Inclusion body myopathy and Paget disease is linked to a novel mutation in the VCP gene;Haubenberger;Neurology,2005
5. Pathological consequences of VCP mutations on human striated muscle;Hubbers;Brain,2006
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