KCNN2

Publications

Balint B et al. KCNN2 mutation in autosomal-dominant tremulous myoclonus-dystonia. Europ. J. Neurol. 2020;27:1471-1477. PMID: 32212350.

Mochel FM et al. Variants in the SK2 channel gene (KCNN2) lead to dominant neurodevelopmental movement disorders. Brain. 2020;143:3564-3573. PMID: 33242881.

Raghuram V et al. Assessment of mutations in KCNN2 and ZNF135 to patient neurological symptoms. Neuroreport. 2017;28(7):375-379. PMID: 28240725.