A GABRB3 promoter haplotype associated with childhood absence epilepsy impairs transcriptional activity
Author(s) -
L Urak,
Martha Feucht,
Nahid Karimian Fathi,
Kurt Hornik,
Karoline Fuchs
Publication year - 2006
Publication title -
human molecular genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.811
H-Index - 276
eISSN - 1460-2083
pISSN - 0964-6906
DOI - 10.1093/hmg/ddl397
Subject(s) - biology , haplotype , epilepsy , genetics , childhood absence epilepsy , promoter activity , gene , promoter , allele , neuroscience , gene expression
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