A novel SLC2A1 mutation linking hemiplegic migraine with alternating hemiplegia of childhood

Cephalalgia

Volumn 35, Issue 1, 2015, Pages 10-15

  Weller, Claudia M ^a   Leen, Wilhelmina G ^b   Neville, Brian G R ^c   Duncan, John S ^d   De Vries, Boukje ^a   Geilenkirchen, Marije A ^a   Haan, Joost ^c,e   Kamsteeg, Erik Jan ^f   Ferrari, Michel D ^a   Van Den Maagdenberg, Arn M J M ^a   Willemsen, Michèl A A P ^b   Scheffer, Hans ^f   Terwindt, Gisela M ^a  

^a LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

^b RADBOUD UNIVERSITY   (Netherlands)

^c UNIVERSITY COLLEGE LONDON   (United Kingdom)

^d UNIVERSITY COLLEGE LONDON   (United Kingdom)

^e RIJNLAND HOSPITAL   (Netherlands)

^f RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

Alternating hemiplegia of childhood (AHC); Exercise induced dystonia; GLUT1 deficiency syndrome; Hemiplegic migraine (HM); SLC2A1 gene

Indexed keywords

ARGININE; GLYCINE; GLUCOSE TRANSPORTER 1; SLC2A1 PROTEIN, HUMAN;

ALTERNATING HEMIPLEGIA OF CHILDHOOD; ARTICLE; ATP1A3 GENE; CLINICAL ARTICLE; GENE MUTATION; GENETIC SCREENING; HEMIPLEGIA; HEMIPLEGIC MIGRAINE; HUMAN; MUTATOR GENE; PHENOTYPE; SLC2A1 GENE; SYMPTOMATOLOGY; ADOLESCENT; ADULT; CASE REPORT; CHILD; FEMALE; GENETICS; MIGRAINE WITH AURA; MULTIPLEX POLYMERASE CHAIN REACTION; MUTATION; NUCLEOTIDE SEQUENCE; ONSET AGE; YOUNG ADULT;

ADOLESCENT; ADULT; AGE OF ONSET; CHILD; DNA MUTATIONAL ANALYSIS; FEMALE; GLUCOSE TRANSPORTER TYPE 1; HEMIPLEGIA; HUMANS; MIGRAINE WITH AURA; MULTIPLEX POLYMERASE CHAIN REACTION; MUTATION; YOUNG ADULT;

EID: 84927762103     PISSN: 03331024     EISSN: 14682982     Source Type: Journal    
DOI: 10.1177/0333102414532379     Document Type: Article

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