Exclusion of the juvenile myoclonic epilepsy gene EFHC1 as the cause of migraine on chromosome 6, but association to two rare polymorphisms in MEP1A and RHAG

Neuroscience Letters

Volumn 396, Issue 2, 2006, Pages 137-142

  Norberg, Anna ^a   Forsgren, Lars ^b   Holmberg, Dan ^a   Holmberg, Monica ^a  

^a UMEÅ UNIVERSITY   (Sweden)

^b UMEÅ UNIVERSITY HOSPITAL   (Sweden)

Author keywords

Association; Candidate genes; EFHC1; MEP1A; Migraine; RHAG

Indexed keywords

GLYCOPROTEIN; INTERLEUKIN 17; MEP1A; MEPRIN; PROTEIN EFHC1; PROTEIN RHAG; UNCLASSIFIED DRUG;

ARTICLE; BRAIN MAPPING; CHROMOSOME 6; DISEASE ASSOCIATION; DISEASE COURSE; GENE FUNCTION; GENE IDENTIFICATION; GENE MUTATION; GENE SEGREGATION; GENETIC CORRELATION; GENETIC PREDISPOSITION; HAPLOTYPE; HUMAN; MIGRAINE; MUTATIONAL ANALYSIS; MYOCLONUS EPILEPSY; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM;

BLOOD PROTEINS; CALCIUM-BINDING PROTEINS; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 6; DNA MUTATIONAL ANALYSIS; FEMALE; GENE DELETION; GENETIC PREDISPOSITION TO DISEASE; HETEROZYGOTE; HUMANS; INCIDENCE; MALE; MEMBRANE GLYCOPROTEINS; METALLOENDOPEPTIDASES; MIGRAINE DISORDERS; MULTIGENE FAMILY; PEDIGREE; POLYMORPHISM, SINGLE NUCLEOTIDE; SWEDEN;

EID: 33244479015     PISSN: 03043940     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neulet.2005.11.039     Document Type: Article

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