One family, one gene and three phenotypes: A novel VCP (valosin-containing protein) mutation associated with myopathy with rimmed vacuoles, amyotrophic lateral sclerosis and frontotemporal dementia

Title
One family, one gene and three phenotypes: A novel VCP (valosin-containing protein) mutation associated with myopathy with rimmed vacuoles, amyotrophic lateral sclerosis and frontotemporal dementia
Authors
Keywords
Inclusion body myopathy, Frontotemporal dementia, Amyotrophic lateral sclerosis, VCP, Valosin-containing protein
Journal
JOURNAL OF THE NEUROLOGICAL SCIENCES
Volume 368, Issue -, Pages 352-358
Publisher
Elsevier BV
Online
2016-07-22
DOI
10.1016/j.jns.2016.07.048

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