Hereditary spastic paraplegia caused by a mutation in the VCP gene
Author:
Publisher
Oxford University Press (OUP)
Subject
Neurology (clinical)
Link
http://academic.oup.com/brain/article-pdf/135/12/e223/794221/aws201.pdf
Reference16 articles.
1. Inclusion body myopathy and frontotemporal dementia caused by a novel VCP mutation
2. Strumpellin is a novel valosin-containing protein binding partner linking hereditary spastic paraplegia to protein aggregation diseases
3. The Arp2/3 Activator WASH Controls the Fission of Endosomes through a Large Multiprotein Complex
4. An evaluation of neurophysiological criteria used in the diagnosis of motor neuron disease
5. A Brazilian family with hereditary inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia
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