The potential role of CAMSAP1L1 in symptomatic epilepsy.

doi:10.1016/j.neulet.2013.10.020

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Article

The potential role of CAMSAP1L1 in symptomatic epilepsy.

Neuroscience letters - 27 Nov 2013

Zhang Shuai, Kwan Patrick, Baum Larry

Abstract excerpt

In a recent genome-wide association study (GWAS) of symptomatic epilepsy in the Chinese population, the most significant single nucleotide polymorphism (SNP) allele was rs2292096 [G] (P=1.0×10(-8), odds ratio [OR]=0.63), in the CAMSAP1L1 gene (also known as CAMSAP2). Here, we report that rs229209...

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PMID: 24148305
DOI: 10.1016/j.neulet.2013.10.020

Genes

CAMSAP2

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-24148305-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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