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Article

Impact of missense TSBP1 variants on the susceptibility to coronary heart disease.

Gene - 20 Feb 2024

Yang Wei, Li Xuguang, Li Xuemei, Hu Baoping, Xu Shilin, Zhang Hengxun, Wang Yuhe, Jin Tianbo, He Yongjun

Abstract excerpt

BACKGROUND: A genome-wide association study has recognized C6orf10-BTNL2 polymorphism in coronary artery disease. The goal of this study was to explore the potential correlation of nine missense TSBP1 variants with coronary heart disease (CHD) risk in the Chinese Han population. METHODS: Nine TSBP1 missense single nucleotide polymorphisms (SNPs) were selected for genotyping by the Agena MassARRAY platform. Odds...

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Source

Identifiers

PMID: 38042215
DOI: 10.1016/j.gene.2023.148042

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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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