Variable clinical expression of mutations in the P/Q-type calcium channel gene in familial hemiplegic migraine

Neurology

Volumn 50, Issue 4, 1998, Pages 1105-1110

  Terwindt, G M ^a   Ophoff, R A ^a   Haan, J ^a,b   Vergouwe, M N ^a   Van Eijk, R ^a   Frants, R R ^c   Ferrari, M D ^a  

^a LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

^b RIJNLAND HOSPITAL   (Netherlands)

^c NONE

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM CHANNEL;

ARTICLE; AUTOSOMAL DOMINANT DISORDER; CLINICAL ARTICLE; FAMILIAL DISEASE; FEMALE; GENE EXPRESSION; GENE MUTATION; GENOTYPE; HEMIPLEGIA; HUMAN; MALE; MIGRAINE; MISSENSE MUTATION; PEDIGREE; PHENOTYPE; PRIORITY JOURNAL; TRINUCLEOTIDE REPEAT;

EID: 0031896548     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/wnl.50.4.1105     Document Type: Article

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