Genetic variants of the NOTCH3 gene in migraine - A mutation analysis and association study

Cephalalgia

Volumn 26, Issue 2, 2006, Pages 158-161

  Schwaag, S ^a   Evers, S ^a   Schirmacher, A ^a   Stogbauer F ^a   Ringelstein, E B ^a   Kuhlenbaumer G ^a  

^a UNIVERSITY OF MÜNSTER   (Germany)

Author keywords

Association study; CADASIL; Migraine; NOTCH3

Indexed keywords

NOTCH3 RECEPTOR;

ADOLESCENT; ADULT; ARTICLE; CONTROLLED STUDY; DISEASE ASSOCIATION; DNA SEQUENCE; EXON; FEMALE; GENE MUTATION; GENETIC POLYMORPHISM; GENETIC VARIABILITY; HUMAN; MAJOR CLINICAL STUDY; MALE; MIGRAINE; NUCLEOTIDE SEQUENCE; SINGLE NUCLEOTIDE POLYMORPHISM;

ADOLESCENT; ADULT; DNA MUTATIONAL ANALYSIS; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENETIC SCREENING; GERMANY; HUMANS; MALE; MIDDLE AGED; MIGRAINE DISORDERS; MUTATION; POLYMORPHISM, GENETIC; POLYMORPHISM, SINGLE NUCLEOTIDE; PREVALENCE; RECEPTORS, NOTCH; RISK ASSESSMENT; RISK FACTORS; VARIATION (GENETICS);

EID: 33644951394     PISSN: 03331024     EISSN: 14682982     Source Type: Journal    
DOI: 10.1111/j.1468-2982.2005.01007.x     Document Type: Article

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