Alternating hemiplegia of childhood: No mutations in the glutamate transporter EAAT1

Neuropediatrics

Volumn 37, Issue 5, 2006, Pages 302-304

  De Vries, B ^a   Haan, Joost ^a,b   Stam, A H ^a   Vanmolkot, K R J ^a   Stroink, H ^c   Laan, L A E M ^a   Gill, D S ^d   Pascual, J ^e   Frants, R R ^a   Van Den Maagdenberg, A M J M ^a   Ferrari, M D ^a  

^a LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

^b RIJNLAND HOSPITAL   (Netherlands)

^c CPRLab   (Netherlands)

^d CHILDREN S HOSPITAL AT WESTMEAD   (Australia)

^e HOSPITAL UNIVERSITARIO DE SALAMANCA   (Spain)

Author keywords

EAAT1; Familial hemiplegic migraine; SLC1A3

Indexed keywords

EXCITATORY AMINO ACID TRANSPORTER 1; GLUTAMATE TRANSPORTER;

ARTICLE; ATAXIA; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; DISEASE COURSE; DNA FLANKING REGION; EXON; FAMILIAL HEMIPLEGIC MIGRAINE; GENE FUNCTION; GENE MUTATION; GENETIC ANALYSIS; GENETIC ASSOCIATION; HEADACHE; HEMIPLEGIA; HUMAN; MUTATIONAL ANALYSIS; PRIORITY JOURNAL; SEIZURE;

ADOLESCENT; CHILD; DNA MUTATIONAL ANALYSIS; EXCITATORY AMINO ACID TRANSPORTER 1; FEMALE; HEMIPLEGIA; HUMANS; MUTATION;

EID: 33846640135     PISSN: 0174304X     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2006-924609     Document Type: Article

References (11)

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