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Article

EGLN2 and RNF150 genetic variants are associated with chronic obstructive pulmonary disease risk in the Chinese population.

International journal of chronic obstructive pulmonary disease - 1 Jan 2015

Ding Yipeng, Niu Huan, Yang Hua, Sun Pei, Chen Yu, Duan Mengling, Xu Dongchuan, Xu Junxue, Jin Tianbo

Abstract excerpt

PURPOSE: Chronic obstructive pulmonary disease (COPD) is a major and an increasingly prevalent health problem worldwide. It has been reported that genetic variation may play a role in the development and severity of COPD. The purpose of this study was to investigate whether single nucleotide polymorphisms in multiple genetic variants were associated with COPD in a Chinese population from Hainan province. METHODS:...

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Source

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Identifiers

PMID: 25609945
DOI: 10.2147/COPD.S73031
PMCID: PMC4298296

Genes

EGLN2

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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