The genetic spectrum of a population-based sample of familial hemiplegic migraine

Brain

Volumn 130, Issue 2, 2007, Pages 346-356

  Thomsen, Lise Lykke ^a   Kirchmann, M ^a   Bjornsson, A ^b   Stefansson, H ^b   Jensen, R M ^a   Fasquel, A C ^b   Petursson, H ^b   Stefansson, M ^b   Frigge, M L ^b   Kong, A ^b   Gulcher, J ^b   Stefansson, K ^b   Olesen, J ^a  

^a UNIVERSITY OF COPENHAGEN   (Denmark)

^b DECODE GENETICS   (Iceland)

Author keywords

Familial hemiplegic migraine; Genetics; Genome scan; Loci; Mutations

Indexed keywords

ADENOSINE TRIPHOSPHATASE (POTASSIUM SODIUM); CALCIUM CHANNEL; SODIUM CHANNEL;

ADOLESCENT; ADULT; AGED; ARTICLE; DENMARK; DIAGNOSTIC PROCEDURE; EXON; FAMILIAL HEMIPLEGIC MIGRAINE; FAMILY; FEMALE; GENE LOCUS; GENETIC LINKAGE; GENETIC SCREENING; HUMAN; INTERNATIONAL CLASSIFICATION OF DISEASES; MAJOR CLINICAL STUDY; MALE; MISSENSE MUTATION; MUTATIONAL ANALYSIS; NEUROLOGIC EXAMINATION; PHYSICAL EXAMINATION; POPULATION GENETICS; PRIORITY JOURNAL; PROMOTER REGION; SCHOOL CHILD;

ADOLESCENT; ADULT; AGED; AGED, 80 AND OVER; CALCIUM CHANNELS; CHILD; DNA MUTATIONAL ANALYSIS; FEMALE; GENOTYPE; HEMIPLEGIA; HUMANS; LINKAGE (GENETICS); MALE; MIDDLE AGED; MIGRAINE WITH AURA; MUTATION; NA(+)-K(+)-EXCHANGING ATPASE; PEDIGREE;

EID: 33846620591     PISSN: 00068950     EISSN: 14602156     Source Type: Journal    
DOI: 10.1093/brain/awl334     Document Type: Article

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