Mutation analysis of VCP in British familial and sporadic amyotrophic lateral sclerosis patients

Neurobiology of Aging

Volumn 33, Issue 11, 2012, Pages 2721.e1-2721.e2

  Miller, Jack W ^a   Smith, Bradley N ^a   Topp, Simon D ^a   Al Chalabi, Ammar ^a   Shaw, Christopher E ^a   Vance, Caroline ^a  

^a KING'S COLLEGE LONDON   (United Kingdom)

Author keywords

Amyotrophic lateral sclerosis; Familial ALS; Motor neuron disease; Mutation; VCP gene

Indexed keywords

DNA; VALOSIN CONTAINING PROTEIN;

AMYOTROPHIC LATERAL SCLEROSIS; ARTICLE; CELL INCLUSION; COHORT ANALYSIS; DISEASE PREDISPOSITION; DNA BINDING; EXON; FRONTOTEMPORAL DEMENTIA; GENE MUTATION; GENE SEQUENCE; GENETIC ANALYSIS; GENETIC CODE; GENETIC IDENTIFICATION; MUTATIONAL ANALYSIS; NEUROLOGIC DISEASE; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; UBIQUITINATION;

EID: 84865595326     PISSN: 01974580     EISSN: 15581497     Source Type: Journal    
DOI: 10.1016/j.neurobiolaging.2012.06.003     Document Type: Article

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