Association analysis of STX1A gene variants in common forms of migraine

Cephalalgia

Volumn 32, Issue 3, 2012, Pages 203-212

  Tropeano, Maria ^a   Wöber Bingöl, Çiçek ^b   Karwautz, Andreas ^b   Wagner, Gudrun ^b   Vassos, Evangelos ^a   Campos De Sousa, Sara ^a   Graggaber, Andrea ^b   Zesch, Heidi E ^b   Kienbacher, Christian ^b   Natriashvili, Sofia ^b   Kanbur, Incifer ^b   Wöber, Christian ^b   Collier, David A ^a  

^a KING'S COLLEGE LONDON   (United Kingdom)

^b MEDICAL UNIVERSITY OF VIENNA   (Austria)

Author keywords

genetics; ion channels; Migraine; SNP; STX1A

Indexed keywords

POTASSIUM CHANNEL; SYNTAXIN 1A; TWIK RELATED SPINAL CORD POTASSIUM CHANNEL; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; ARTICLE; CALCIUM SIGNALING; CHILD; CONTROLLED STUDY; CYTOPLASM; FEMALE; GENE LOCUS; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC VARIABILITY; HAPLOTYPE; HEREDITY; HUMAN; MAJOR CLINICAL STUDY; MALE; MIGRAINE; MIGRAINE WITHOUT AURA; PRESCHOOL CHILD; SCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM;

ADOLESCENT; CASE-CONTROL STUDIES; CHILD; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENETIC VARIATION; GENOME-WIDE ASSOCIATION STUDY; GENOTYPE; HUMANS; MALE; MIGRAINE DISORDERS; PEDIGREE; SYNTAXIN 1; YOUNG ADULT;

EID: 84856931319     PISSN: 03331024     EISSN: 14682982     Source Type: Journal    
DOI: 10.1177/0333102411433300     Document Type: Article

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