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For: Mary L, Nourisson E, Feger C, Laugel V, Chaigne D, Keren B, Afenjar A, Billette T, Trost D, Cieuta-Walti C, Gerard B, Piton A, Schaefer E. Pathogenic variants in KCNQ2 cause intellectual deficiency without epilepsy: Broadening the phenotypic spectrum of a potassium channelopathy. Am J Med Genet A 2021;185:1803-15. [PMID: 33754465 DOI: 10.1002/ajmg.a.62181] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 3.0] [Reference Citation Analysis]
Number Citing Articles
1 Gribkoff VK, Winquist RJ. Potassium channelopathies associated with epilepsy-related syndromes and directions for therapeutic intervention. Biochem Pharmacol 2023;208:115413. [PMID: 36646291 DOI: 10.1016/j.bcp.2023.115413] [Reference Citation Analysis]
2 <i>KCNQ2</i>- and <i>KCNQ3</i>-Associated Epilepsy. 2022. [DOI: 10.1017/9781009278270] [Reference Citation Analysis]
3 Miceli F, Millevert C, Soldovieri MV, Mosca I, Ambrosino P, Carotenuto L, Schrader D, Lee HK, Riviello J, Hong W, Risen S, Emrick L, Amin H, Ville D, Edery P, de Bellescize J, Michaud V, Van-gils J, Goizet C, Willemsen MH, Kleefstra T, Møller RS, Bayat A, Devinsky O, Sands T, Korenke GC, Kluger G, Mefford HC, Brilstra E, Lesca G, Milh M, Cooper EC, Taglialatela M, Weckhuysen S. KCNQ2 R144 variants cause neurodevelopmental disability with language impairment and autistic features without neonatal seizures through a gain-of-function mechanism. eBioMedicine 2022;81:104130. [DOI: 10.1016/j.ebiom.2022.104130] [Reference Citation Analysis]
4 Singh SP, William M, Malavia M, Chu X. Behavior of KCNQ Channels in Neural Plasticity and Motor Disorders. Membranes 2022;12:499. [DOI: 10.3390/membranes12050499] [Reference Citation Analysis]
5 Arredondo K, Myers C, Hansen-Kiss E, Mathew MT, Jayaraman V, Siemon A, Bartholomew D, Herman GE, Mori M. Phenotypic Spectrum in a Family Sharing a Heterozygous KCNQ3 Variant. J Child Neurol 2022;:8830738221089741. [PMID: 35384780 DOI: 10.1177/08830738221089741] [Reference Citation Analysis]
6 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]
7 Vanoye CG, Desai RR, Ji Z, Adusumilli S, Jairam N, Ghabra N, Joshi N, Fitch E, Helbig K, Mcknight D, Lindy A, Zou F, Helbig I, Cooper E, George AL. High-throughput Evaluation of Epilepsy-associated KCNQ2 Variants Reveals Functional and Pharmacological Heterogeneity.. [DOI: 10.1101/2021.10.18.464842] [Reference Citation Analysis]