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Paper Details

Novel mutation in VCP gene causes atypical amyotrophic lateral sclerosis.
Neurology
54
2012
FALS, IBMPFD, Illumina single nucleotide polymorphism chips, Paget disease of the bone, R155C, R159C, VCP, VCP gene, VCP mutation, VCP mutations, VCP-associated disease, amyotrophic lateral sclerosis, atypical amyotrophic lateral sclerosis, familial amyotrophic lateral sclerosis, frontotemporal dementia, inclusion body myopathy, motor neuron disease, p, p.R155C, p.R159C, p.R191G, sporadic amyotrophic lateral sclerosis, valosin-containing protein

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Release 1.2