Article
Genetic heterogeneity of familial hemiplegic migraine.
American journal of human genetics - 1 Dec 1994
Joutel A, Ducros A, Vahedi K, Labauge P, Delrieu O, Pinsard N, Mancini J, Ponsot G, Gouttière F, Gastaut J L
Abstract excerpt
Familial hemiplegic migraine (FHM) is an autosomal dominant variety of migraine with aura. We previously mapped a gene responsible for this disorder to the short arm of chromosome 19, within a 30-cM interval bracketed by D19S216 and D19S215. Linkage analysis conducted on two large pedigrees did n...
Topics
- Ataxia
- Chi-Square Distribution
- Chromosome Mapping
- Chromosomes, Human, Pair 19
- Female
- Genetic Linkage
- Genetic Markers
- Genetic Variation
- Humans
- Male
- Migraine Disorders
- Nystagmus, Pathologic
- Pedigree
