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Losing your inhibitions: a mutation in the α1 subunit of the GABA A receptor causes autosomal dominant juvenille myoclonic epilepsy
Author(s) -
Brunham LR
Publication year - 2002
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1034/j.1399-0004.2002.620402_4.x
Subject(s) - childhood absence epilepsy , medicine , genetics , epilepsy , biology , psychiatry