2 Article(s)Download |
PMID | Title | Pub. Year | #Total Relationships |
| 1 | 22303015 | GABRB3 mutation, G32R, associated with childhood absence epilepsy alters α1β3γ2L γ-aminobutyric acid type A (GABAA) receptor expression and channel gating. | 2012 Apr 6 | 1 |
| 2 | 16500955 | Structural motif-based homology modeling of CYP27A1 and site-directed mutational analyses affecting vitamin D hydroxylation. | 2006 May 15 | 1 |