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Article

CACNA1I is not associated with childhood absence epilepsy in the Chinese Han population.

Pediatric neurology - 1 Sept 2006

Wang Juli, Zhang Yuehua, Liang Jianmin, Pan Hong, Wu Husheng, Xu Keming, Liu Xiaoyan, Jiang Yuwu, Shen Yan, Wu Xiru

Abstract excerpt

This study investigated whether the T-type calcium channel gene CACNA1I causes susceptibility in the Chinese Han population to childhood absence epilepsy, a form of idiopathic generalized seizure disorder. For this investigation, we searched for mutations in the 35 exons and exon-intron boundaries of the CACNA1I gene in 50 Han Chinese patients with childhood absence epilepsy. Seventeen single nucleotide...

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Identifiers

PMID: 16939858
DOI: 10.1016/j.pediatrneurol.2006.03.006

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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