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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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| Publicat a: | Int J Chron Obstruct Pulmon Dis |
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| Autors principals: | , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Dove Medical Press
2015
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4298296/ https://ncbi.nlm.nih.gov/pubmed/25609945 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/COPD.S73031 |
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