articleNeuronDec 1, 2010NLBRONZE OA

Exome Sequencing Reveals VCP Mutations as a Cause of Familial ALS

JOJanel O. JohnsonJMJessica MandrioliMBMichael BenatarYAYevgeniya AbramzonVMVivianna M. Van Deerlin

National Institutes of Health · University of Modena and Reggio Emilia · +17 more institutions

PubMed
Indexed incrossrefpubmed

Abstract

No abstract available for this paper.

Citation impact

1,223
total citations
FWCI
60.31
Percentile
100%
References
43
Citations per year

Authors

36

Topics & keywords

Topics
Keywords
  • Amyotrophic lateral sclerosis
  • Frontotemporal dementia
  • Exome sequencing
  • Ubiquitin
  • Mutation
  • Phenotype
  • Genetics
  • C9orf72
No related works found for this paper.

Funding