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Article

Mutation screening of the PRRT2 gene for benign epilepsy with centrotemporal spikes in Chinese mainland population.

The International journal of neuroscience - 1 Jan 2017

Che Xiang-Qian, Sun Zhan-Fang, Mao Xiao, Xia Kun, Yan Xin-Xiang, Jiang Hong, Shen Lu, Li Nan, Tang Bei-Sha

Abstract excerpt

Proline-rich transmembrane protein 2 gene (PRRT2) mutations are reported to cause common paroxysmal neurological disorders and show a remarkable pleiotropy. Benign epilepsy with centrotemporal spikes (BECTS) is considered to be the most common epilepsy syndrome in childhood. It is placed among the idiopathic localization related epilepsies. Recently, it was reported that a girl with a PRRT2 mutation c.649_650insC...

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Identifiers

PMID: 26954261
DOI: 10.3109/00207454.2015.1136886

Genes

PRRT2

Variants

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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