No association between polymorphisms in the calcium homeostasis modulator 1 gene and mesial temporal lobe epilepsy risk in a Chinese population.

doi:10.1016/j.seizure.2013.11.010

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Article

No association between polymorphisms in the calcium homeostasis modulator 1 gene and mesial temporal lobe epilepsy risk in a Chinese population.

Seizure - 1 Mar 2014

Li Xiang, Wang Yongcai, Gu Jia, Meng Qingming, Gao Yong, Zhao Hongyu, Yin Zhongmin

Abstract excerpt

PURPOSE: Mesial temporal lobe epilepsy (MTLE) is one of the most common forms of epilepsies in adults. The calcium homeostasis modulator 1 gene (CALHM1) has been considered one of the candidate genes that play a role in epileptogenesis due to its function in calcium homeostasis and amyloid β (Aβ) regulation. Recently, the association of a single nucleotide polymorphism (rs11191692) of CALHM1 has been reported to...

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Identifiers

PMID: 24326043
DOI: 10.1016/j.seizure.2013.11.010

Genes

CALHM1

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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