The CACNA1A and ATP1A2 genes are not involved in dominantly inherited migraine with aura

American Journal of Medical Genetics - Neuropsychiatric Genetics

Volumn 141 B, Issue 3, 2006, Pages 250-256

  Kirchmann, Malene ^a   Thomsen, Lise Lykke ^a   Olesen, Jes ^a  

^a UNIVERSITY OF COPENHAGEN   (Denmark)

Author keywords

Familial hemiplegic migraine; Linkage; Migraine; Mutation

Indexed keywords

ARTICLE; ATP1A2 GENE; AUTOSOMAL DOMINANT DISORDER; CACNA1A GENE; CHROMOSOME 1; CHROMOSOME 19; CHROMOSOME 22; CONTROLLED STUDY; DNA FLANKING REGION; EXON; FAMILIAL HEMIPLEGIC MIGRAINE; GENE; GENE MUTATION; HUMAN; INTRON; LINKAGE ANALYSIS; MAJOR CLINICAL STUDY; MIGRAINE WITH AURA; MIGRAINE WITHOUT AURA; PRIORITY JOURNAL; PROMOTER REGION;

CALCIUM CHANNELS; DENMARK; DNA MUTATIONAL ANALYSIS; FAMILY HEALTH; FEMALE; GENES, DOMINANT; GENOTYPE; HUMANS; LOD SCORE; MALE; MIGRAINE WITH AURA; MUTATION; NA(+)-K(+)-EXCHANGING ATPASE;

EID: 33646014750     PISSN: 15524841     EISSN: 1552485X     Source Type: Journal    
DOI: 10.1002/ajmg.b.30277     Document Type: Article

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