Associated Papers
The absence of NIPA2 enhances neural excitability through BK (big potassium) channels.
Liu NN et al.
Cns Neuroscience & Therapeutics, 2019
Does variation in NIPA2 contribute to genetic generalized epilepsy?
Hildebrand MS et al.
Human Genetics, 2014
Functional study of NIPA2 mutations identified from the patients with childhood absence epilepsy.
Xie H et al.
Plos One, 2014
NIPA2 located in 15q11.2 is mutated in patients with childhood absence epilepsy.
Jiang Y et al.
Human Genetics, 2012
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