The role of SLC2A1 in early onset and childhood absence epilepsies

Epilepsy Research

Volumn 105, Issue 1-2, 2013, Pages 229-233

  Muhle, Hiltrud ^a   Helbig, Ingo ^a   Frøslev, Tobias Guldberg ^b   Suls, Arvid ^c,d   von Spiczak, Sarah ^a   Klitten, Laura Line ^b,e   Dahl, Hans Atli ^f   Brusgaard, Klaus ^f,g   Neubauer, Bernd ^h   De Jonghe, Peter ^c,d,i   Tommerup, Niels ^e   Stephani, Ulrich ^a   Hjalgrim, Helle ^b,j   Møller, Rikke Steensbjerre ^b  

^a UNIVERSITY OF KIEL   (Germany)

^b DANISH EPILEPSY CENTRE   (Denmark)

^c DEPARTMENT OF PLANT SYSTEMS BIOLOGY   (Belgium)

^d UNIVERSITY OF ANTWERP   (Belgium)

^e UNIVERSITY OF COPENHAGEN   (Denmark)

^f Amplexa Genetics A/S   (Denmark)

^g ODENSE UNIVERSITY HOSPITAL   (Denmark)

^h JUSTUS LIEBIG UNIVERSITY   (Germany)

ⁱ ANTWERP UNIVERSITY HOSPITAL   (Belgium)

^j UNIVERSITY OF SOUTHERN DENMARK   (Denmark)

more..

Author keywords

Generalized epilepsies; Genetic epilepsies; GLUT1 deficiency; IGE

Indexed keywords

ETHOSUXIMIDE; VALPROIC ACID;

ARTICLE; ATAXIA; CASE REPORT; CHILDHOOD ABSENCE EPILEPSY; CLINICAL FEATURE; DRUG EFFICACY; DYSTONIA; ELECTROENCEPHALOGRAM; EXON; FEMALE; GENE; GENE FUNCTION; GENE MUTATION; GENETIC SCREENING; HUMAN; INTELLECTUAL IMPAIRMENT; LEARNING DISORDER; MALE; MUTATIONAL ANALYSIS; ONSET AGE; PHOTOSENSITIVITY; PRIORITY JOURNAL; SEIZURE; SLC2A1 GENE; STOP CODON; TREATMENT RESPONSE;

ADOLESCENT; AGE OF ONSET; BASE SEQUENCE; COHORT STUDIES; EARLY DIAGNOSIS; EPILEPSY, ABSENCE; FEMALE; GLUCOSE TRANSPORTER TYPE 1; HETEROZYGOTE DETECTION; HUMANS; MALE; MOLECULAR SEQUENCE DATA; MUTATION; YOUNG ADULT;

EID: 84878435749     PISSN: 09201211     EISSN: 18726844     Source Type: Journal    
DOI: 10.1016/j.eplepsyres.2012.11.004     Document Type: Article

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