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Article

[Phenotype study of SCN2A gene related epilepsy].

Zhonghua er ke za zhi = Chinese journal of pediatrics - 2 Jul 2018

Zeng Q, Zhang Y H, Yang X L, Zhang J, Liu A J, Liu X Y, Jiang Y W, Wu X R

Abstract excerpt

Objective: To summarize the phenotype of epileptic children with SCN2A mutations. Methods: Epileptic patients who were treated in the Pediatric Department of Peking University First Hospital from September 2006 to October 2017 and detected with SCN2A mutations by targeted next-generation sequencing were enrolled. Clinical manifestations of all patients were analyzed retrospectively. Results: A total of 21...

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Identifiers

PMID: 29996185
DOI: 10.3760/cma.j.issn.0578-1310.2018.07.009

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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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