Bauer CK et al. Gain-of-Function Mutations in KCNN3 Encoding the Small-Conductance Ca2+-Activated K+ Channel SK3 Cause Zimmermann-Laband Syndrome. Am J Hum Genet. 2019;104(6):1139–1157. PMID: 31155282.
Gripp KW et al. Syndromic disorders caused by gain-of-function variants in KCNH1, KCNK4, and KCNN3—a subgroup of K+ channelopathies. Eur J Hum Genet. 2021;29(9):1-12. PMID: 33594261.
Schwarz M et al. Zimmermann–Laband syndrome in monozygotic twins with a mild neurobehavioral phenotype lacking gingival overgrowth—A case report of a novel KCNN3 gene variant. Am J Medic Genet A. 2022;188(4):1083-1087. PMID: 34907639.
KCNN3