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Cited by in F6Publishing
For: Xiong J, Liu Z, Chen S, Kessi M, Chen B, Duan H, Deng X, Yang L, Peng J, Yin F. Correlation Analyses of Clinical Manifestations and Variant Effects in KCNB1-Related Neurodevelopmental Disorder. Front Pediatr 2021;9:755344. [PMID: 35071126 DOI: 10.3389/fped.2021.755344] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
Number Citing Articles
1 Hiraide T, Akita T, Uematsu K, Miyamoto S, Nakashima M, Sasaki M, Fukuda A, Kato M, Saitsu H. A novel de novo KCNB1 variant altering channel characteristics in a patient with periventricular heterotopia, abnormal corpus callosum, and mild seizure outcome. J Hum Genet 2023;68:25-31. [PMID: 36257979 DOI: 10.1038/s10038-022-01090-5] [Reference Citation Analysis]
2 Veale EL, Golluscio A, Grand K, Graham JM Jr, Mathie A. A KCNB1 gain of function variant causes developmental delay and speech apraxia but not seizures. Front Pharmacol 2022;13:1093313. [PMID: 36618935 DOI: 10.3389/fphar.2022.1093313] [Reference Citation Analysis]
3 Gao K, Lin Z, Wen S, Jiang Y. Potassium channels and epilepsy. Acta Neurol Scand 2022. [PMID: 36225112 DOI: 10.1111/ane.13695] [Reference Citation Analysis]
4 Xiong J, Chen S, Chen B, Zhang W, Chen C, Deng X, He F, Zhang C, Yang L, Wang Y, Peng J, Yin F. A novel KCNQ2 missense variant in non-syndromic intellectual disability causes mild gain-of-function of Kv7.2 channel. Clin Chim Acta 2022:S0009-8981(22)00082-1. [PMID: 35247435 DOI: 10.1016/j.cca.2022.03.001] [Reference Citation Analysis]