No mutations in CACNA1A and ATP1A2 in probands with common types of migraine

Archives of Neurology

Volumn 61, Issue 6, 2004, Pages 926-928

  Jen, Joanna C ^a   Kim, Gilbert W ^a   Dudding, Kristen A ^a   Baloh, Robert W ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATASE (POTASSIUM SODIUM); CALCIUM CHANNEL;

ADOLESCENT; ADULT; ARTICLE; ATAXIA; ATP1A2 GENE; AUTOSOMAL DOMINANT DISORDER; CACNA1A GENE; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; DNA FLANKING REGION; EXON; FEMALE; GENE; GENE AMPLIFICATION; GENE FREQUENCY; GENE MUTATION; GENE SEQUENCE; HEMIPLEGIA; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HUMAN; INTRON; MALE; MIGRAINE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROSPECTIVE STUDY;

ADOLESCENT; ADULT; CALCIUM CHANNELS; CALCIUM CHANNELS, P-TYPE; CALCIUM CHANNELS, Q-TYPE; CHILD; CHILD, PRESCHOOL; FEMALE; HUMANS; MALE; MIDDLE AGED; MIGRAINE DISORDERS; MUTATION; NA(+)-K(+)-EXCHANGING ATPASE; PROSPECTIVE STUDIES;

EID: 2942525883     PISSN: 00039942     EISSN: None     Source Type: Journal    
DOI: 10.1001/archneur.61.6.926     Document Type: Article

References (14)

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