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

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 polymor...

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Detalles Bibliográficos
Autores principales: Ding, Yipeng, Niu, Huan, Yang, Hua, Sun, Pei, Chen, Yu, Duan, Mengling, Xu, Dongchuan, Xu, Junxue, Jin, Tianbo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4298296/
https://www.ncbi.nlm.nih.gov/pubmed/25609945
http://dx.doi.org/10.2147/COPD.S73031

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4298296/
https://www.ncbi.nlm.nih.gov/pubmed/25609945
http://dx.doi.org/10.2147/COPD.S73031

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