E Tournier-Lasserve. Show Affiliations »
Abstract
Entities: Disease Gene
Mesh: See more » Amino Acid SubstitutionCalcium Channels/geneticsCerebellar Ataxia/geneticsHemiplegia/geneticsHumansMigraine Disorders/geneticsPoint Mutation
Substances: See more » CACNA1A protein, humanCalcium Channels
Year: 1999 PMID: 10408526 DOI: 10.1212/wnl.53.1.3
Source DB: PubMed Journal: Neurology ISSN: 0028-3878 Impact factor: 9.910