Genetic TPH2 variants and the susceptibility for migraine: Association of a TPH2 haplotype with migraine without aura

Journal of Neural Transmission

Volumn 117, Issue 11, 2010, Pages 1253-1260

  Jung, Alexander ^a,b   Huge, Andreas ^c   Kuhlenbäumer, Gregor ^a,c   Kempt, Steffi ^a   Seehafer, Tanja ^c   Evers, Stefan ^a   Berger, Klaus ^c   Marziniak, Martin ^a,b  

^a UNIVERSITY HOSPITAL MÜNSTER   (Germany)

^b SAARLAND UNIVERSITY   (Germany)

^c UNIVERSITY OF MÜNSTER   (Germany)

Author keywords

Genetic association study; Migraine; Serotonin; Tryptophan hydroxylase

Indexed keywords

SEROTONIN; TRIPTAN DERIVATIVE; TRYPTOPHAN HYDROXYLASE 2;

ADULT; ARTICLE; CONTROLLED STUDY; FEMALE; GENE FUNCTION; GENETIC ASSOCIATION; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; GENETICS; GENOTYPE; HAPLOTYPE; HOMEOSTASIS; HUMAN; MAJOR CLINICAL STUDY; MALE; MIGRAINE; MIGRAINE WITHOUT AURA; NUCLEOTIDE SEQUENCE; PATHOGENESIS; PRIORITY JOURNAL; SEROTONIN BRAIN LEVEL; SEROTONINERGIC SYSTEM; SINGLE NUCLEOTIDE POLYMORPHISM; TREATMENT RESPONSE; TRYPTOPHAN HYDROXYLASE 2 GENE;

ADULT; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENOME-WIDE ASSOCIATION STUDY; GENOTYPE; HAPLOTYPES; HUMANS; MALE; MIGRAINE DISORDERS; POLYMORPHISM, SINGLE NUCLEOTIDE; TRYPTOPHAN HYDROXYLASE;

EID: 78651253783     PISSN: 03009564     EISSN: 14351463     Source Type: Journal    
DOI: 10.1007/s00702-010-0468-6     Document Type: Article

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