No mutations detected in the INSR gene in a chromosome 19p13 linked migraine pedigree

European Journal of Medical Genetics

Volumn 49, Issue 1, 2006, Pages 57-62

  Curtain, Robert ^a   Tajouri, Lotti ^a   Lea, Rod ^a,b   MacMillan, John ^c   Griffiths, Lyn ^a  

^a GRIFFITH UNIVERSITY   (Australia)

^b VICTORIA UNIVERSITY OF WELLINGTON   (New Zealand)

^c ROYAL CHILDREN'S HOSPITAL   (Australia)

Author keywords

INSR; Migraine; Mutation; SNP; Variation

Indexed keywords

5' UNTRANSLATED REGION; ADULT; AGED; ARTICLE; CHROMOSOME 19P; CLINICAL ARTICLE; DISEASE ASSOCIATION; DNA SEQUENCE; EXON; FAMILY; FEMALE; GENE; GENE MUTATION; GENE SEQUENCE; GENETIC CODE; GENETIC VARIABILITY; HUMAN; MALE; MIGRAINE; MIGRAINE AURA; MUTATIONAL ANALYSIS; PEDIGREE; SINGLE NUCLEOTIDE POLYMORPHISM;

ADULT; AGED; CALCIUM CHANNELS; CHROMOSOMES, HUMAN, PAIR 19; FEMALE; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MALE; MIDDLE AGED; MIGRAINE DISORDERS; MUTATION; PEDIGREE; POLYMORPHISM, SINGLE NUCLEOTIDE; RECEPTOR, INSULIN;

EID: 32244444320     PISSN: 17697212     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ejmg.2005.01.015     Document Type: Article

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