Expansion of the phenotypic spectrum of the CACNA1A T666M mutation: a family with familial hemiplegic migraine type 1, cerebellar atrophy and mental retardation

Cephalalgia. 2008 Apr;28(4):403-7. doi: 10.1111/j.1468-2982.2008.01540.x. Epub 2008 Feb 14.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Atrophy
  • Calcium Channels / genetics*
  • Cerebellar Diseases / genetics*
  • Cerebellar Diseases / pathology
  • Family Health
  • Humans
  • Intellectual Disability / genetics*
  • Intellectual Disability / pathology
  • Middle Aged
  • Migraine with Aura / genetics*
  • Phenotype
  • Point Mutation

Substances

  • CACNA1A protein, human
  • Calcium Channels