Two novel SCN1A mutations identified in families with familial hemiplegic migraine

Cephalalgia

Volumn 34, Issue 13, 2014, Pages 1062-1069

  Weller, Claudia M ^a   Pelzer, Nadine ^a   De Vries, Boukje ^a   López, Mercè Artigas ^b   De Fàbregues, Oriol ^c   Pascual, Julio ^d   Arroyo, María A Ramos ^b   Koelewijn, Stephany C ^a   Stam, Anine H ^a   Haan, Joost ^a,e   Ferrari, Michel D ^a   Terwindt, Gisela M ^a   Van Den Maagdenberg, Arn M J M ^a  

^a LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

^b Instituto de Investigación Sanitaria de Navarra   (Spain)

^c HOSPITAL UNIVERSITARI VALL D HEBRON   (Spain)

^d HOSPITAL UNIVERSITARIO CENTRAL DE ASTURIAS   (Spain)

^e RIJNLAND HOSPITAL   (Netherlands)

Author keywords

familial hemiplegic migraine; ion channel defects; Migraine; SCN1A gene

Indexed keywords

AMINO ACID; SODIUM CHANNEL NAV1.1; SCN1A PROTEIN, HUMAN;

ADULT; AGED; ARTICLE; ATP1A2 GENE; CACNA1A GENE; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; DISEASE SEVERITY; EXON; FAMILIAL HEMIPLEGIC MIGRAINE; FEMALE; GENE; GENE IDENTIFICATION; GENE MUTATION; GENE SEQUENCE; GENETIC ANALYSIS; GENETIC SCREENING; HUMAN; MALE; MIDDLE AGED; MISSENSE MUTATION; POINT MUTATION; PROTEIN DOMAIN; PRRT2 GENE; VERY ELDERLY; YOUNG ADULT; ADOLESCENT; AMINO ACID SEQUENCE; CASE REPORT; CHILD; GENETICS; MIGRAINE WITH AURA; MOLECULAR GENETICS; MUTATION; NUCLEOTIDE SEQUENCE; ONSET AGE; PEDIGREE;

ADOLESCENT; ADULT; AGE OF ONSET; AGED; AMINO ACID SEQUENCE; CHILD; DNA MUTATIONAL ANALYSIS; FEMALE; HUMANS; MALE; MIDDLE AGED; MIGRAINE WITH AURA; MOLECULAR SEQUENCE DATA; MUTATION; NAV1.1 VOLTAGE-GATED SODIUM CHANNEL; PEDIGREE; YOUNG ADULT;

EID: 84909633098     PISSN: 03331024     EISSN: 14682982     Source Type: Journal    
DOI: 10.1177/0333102414529195     Document Type: Article

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