Clinical Study of 30 Novel KCNQ2 Variants/Deletions in KCNQ2-Related Disorders

Clinical Study of 30 Novel KCNQ2 Variants/Deletions in KCNQ2-Related Disorders

BackgroundKCNQ2-related disorder is typically characterized as neonatal onset seizure and epileptic encephalopathy. The relationship between its phenotype and genotype is still elusive. This study aims to provide clinical features, management, and prognosis of patients with novel candidate variants...

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Bibliographic Details
Main Authors:	Tiantian Xiao, Xiang Chen, Yan Xu, Huiyao Chen, Xinran Dong, Lin Yang, Bingbing Wu, Liping Chen, Long Li, Deyi Zhuang, Dongmei Chen, Yuanfeng Zhou, Huijun Wang, Wenhao Zhou
Format:	Article
Language:	English
Published:	Frontiers Media S.A. 2022-04-01
Series:	Frontiers in Molecular Neuroscience
Subjects:	KCNQ2 Kv7.2 newborn epilepsy epileptic encephalopathy
Online Access:	https://www.frontiersin.org/articles/10.3389/fnmol.2022.809810/full

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