CACNA1A R1347Q: A frequent recurrent mutation in hemiplegic migraine

Clinical Genetics

Volumn 74, Issue 5, 2008, Pages 481-485

  Stam, A H ^a   Vanmolkot, K R J ^a   Kremer, H P H ^b   Gartner J ^c   Brown, J ^d   Leshinsky Silver, E ^e   Gilad, R ^e   Kors, E E ^a   Frankhuizen, W S ^a   Ginjaar, H B ^a   Haan, J ^a,f   Frants, R R ^a   Ferrari, R R ^a   Van Den Maagdenberg, A M J M ^a   Terwindt, Gisela M ^a  

^a LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

^b RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^c UNIVERSITY OF GÖTTINGEN   (Germany)

^d QUEEN ELIZABETH HOSPITAL   (United Kingdom)

^e WOLFSON MEDICAL CENTER   (Israel)

^f RIJNLAND HOSPITAL   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

ACETAZOLAMIDE; ARGININE; CALCIUM CHANNEL; FAMILIAL HEMIPLEGIC MIGRAINE TYPE 1 PROTEIN; GLUTAMINE; UNCLASSIFIED DRUG; VALPROIC ACID;

ADOLESCENT; ADULT; AGED; ARTICLE; ATAXIA; CLINICAL ARTICLE; CONSCIOUSNESS DISORDER; DISEASE EXACERBATION; DISEASE SEVERITY; EPILEPSY; FAMILY STUDY; FEMALE; GENE FREQUENCY; GENE IDENTIFICATION; GENETIC SCREENING; GENOTYPE PHENOTYPE CORRELATION; HEMIPLEGIC MIGRAINE; HETEROZYGOTE; HUMAN; HUMAN CELL; MALE; MIGRAINE WITH AURA; MISSENSE MUTATION; MUTATIONAL ANALYSIS; NEUROLOGIC EXAMINATION; NUCLEAR MAGNETIC RESONANCE IMAGING; NUCLEOTIDE SEQUENCE; PEDIGREE ANALYSIS; PRIORITY JOURNAL;

ADOLESCENT; AGED; CALCIUM CHANNELS; DNA MUTATIONAL ANALYSIS; FEMALE; GENOTYPE; HAPLOTYPES; HUMANS; MALE; MIDDLE AGED; MIGRAINE WITH AURA; MODELS, BIOLOGICAL; MUTATION; PEDIGREE; PHENOTYPE;

EID: 51149087575     PISSN: 00099163     EISSN: 13990004     Source Type: Journal    
DOI: 10.1111/j.1399-0004.2008.00996.x     Document Type: Article

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