Associated Papers
Identification of a novel KCNT2 variant in a family with developmental and epileptic encephalopathies: a case report and literature review.
Cui F et al.
Frontiers in Genetics, 2024
Recurrent KCNT2 missense variants affecting p.Arg190 result in a recognizable phenotype.
Jackson A et al.
American Journal of Medical Genetics. Part A, 2021
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