Absence of known familial hemiplegic migraine (FHM) mutations in the CACNA1A gene in patients with common migraine: Implications for genetic testing

Clinical Chemistry and Laboratory Medicine

Volumn 41, Issue 3, 2003, Pages 272-275

  Wieser, Thomas ^a   Mueller, Christoph ^a   Evers, Stefan ^b   Zierz, Stephan ^a   Deufel, Thomas ^c  

^a MARTIN LUTHER UNIVERSITY HALLE WITTENBERG   (Germany)

^b UNIVERSITY HOSPITAL MÜNSTER   (Germany)

^c JENA UNIVERSITY HOSPITAL   (Germany)

Author keywords

CACNA1A gene; Common migraine; Familial hemiplegic migraine; Mutation analysis

Indexed keywords

CACNA1A PROTEIN; GENE PRODUCT; UNCLASSIFIED DRUG;

ALLELE; ARTICLE; CHROMOSOME 19; CONTROLLED STUDY; DISEASE CLASSIFICATION; EXON; FAMILY HISTORY; FEASIBILITY STUDY; GENE MUTATION; GENETIC ANALYSIS; GENETIC LINKAGE; GENETIC SCREENING; HEMIPLEGIA; HUMAN; HUMAN CELL; HYPOTHESIS; MAJOR CLINICAL STUDY; MEDICAL DECISION MAKING; MIGRAINE; MOLECULAR MECHANICS; PATHOGENESIS; PATHOPHYSIOLOGY; PHENOTYPE; PRIORITY JOURNAL; SINGLE STRAND CONFORMATION POLYMORPHISM;

CALCIUM CHANNELS; CHROMOSOMES, HUMAN, PAIR 19; EXONS; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GERMANY; HEMIPLEGIA; HUMANS; MALE; MIGRAINE WITH AURA; MIGRAINE WITHOUT AURA; PEDIGREE; POINT MUTATION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL;

EID: 0037257098     PISSN: 14346621     EISSN: None     Source Type: Journal    
DOI: 10.1515/CCLM.2003.042     Document Type: Article

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