GABRB3 mutation, G32R, associated with childhood absence epilepsy alters α1β3γ2L γ-aminobutyric acid type A (GABA A) receptor expression and channel gating

Katharine N. Gurba, Ciria C. Hernandez, Ningning Hu, Robert L. Macdonald

Research output: Contribution to journal › Article › peer-review

42 Scopus citations

Fingerprint

Dive into the research topics of 'GABRB3 mutation, G32R, associated with childhood absence epilepsy alters α1β3γ2L γ-aminobutyric acid type A (GABA A) receptor expression and channel gating'. Together they form a unique fingerprint.

Medicine & Life Sciences

Chemical Compounds