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Article

Gene-wide tagging study of the association between KCNT1 polymorphisms and the susceptibility and efficacy of genetic generalized epilepsy in Chinese population.

CNS neuroscience & therapeutics - 1 Feb 2014

Qu Jian, Zhang Ying, Yang Zhi-Quan, Mao Xiao-Yuan, Zhou Bo-Ting, Yin Ji-Ye, He Hui, Li Xiang-Ping, Long Hong-Yu, Lv Nan, Xu Xiao-Jing, Xiao Bo, Zhang Yu, Tang Qiang, Hu Dong-Li, Zhou Hong-Hao, Liu Zhao-Qian

Abstract excerpt

AIMS: The causes of genetic generalized epilepsies (GGEs) are still uncertain now. Some studies found that the human potassium channel, subfamily T, member 1 (KCNT1) is the candidate gene causing malignant migrating partial seizures of infancy and autosomal dominant nocturnal frontal lobe epilepsy which are all rare genetic generalized epilepsies. The aims of this study were going to evaluate the association...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Open in PubMed Open full text

Identifiers

PMID: 24279416
DOI: 10.1111/cns.12169
PMCID: PMC6493076

Genes

KCNT1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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