Gain-of-function KCNJ6 Mutation in a Severe Hyperkinetic Movement Disorder Phenotype
Keywords: ماوس بافندگی; GIRK; G protein-gated inwardly rectifying K+; KIR; inwardly rectifying potassium; SNc; substantia nigra compacta; WES; whole-exome sequencing; KCNJ6; weaver mouse; movement disorder; channelopathy; inward rectifier; KIR3;