Kelienne Verdier

Epileptic encephalopathy de novo<i>GABRB</i>mutations impair γ‐aminobutyric acid type A receptor function

Vaishali Satpute Janve, Ciria C. Hernández, Kelienne Verdier et al. · Annals of Neurology · 2016 · 82 citations · Full text

Overexpressing wild‐type γ2 subunits rescued the seizure phenotype in <i>Gabrg2</i>^{<i>+/Q390X</i>} Dravet syndrome mice

Xuan Huang, Chengwen Zhou, Mengnan Tian et al. · Epilepsia · 2017 · 24 citations · Full text

Beyond Epilepsy and Autism: Disruption of GABRB3 Causes Ocular Hypopigmentation

Ryan Delahanty, Yanfeng Zhang, Terry Jo Bichell et al. · Cell Reports · 2016 · 18 citations · Full text