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MUC5B and Idiopathic Pulmonary Fibrosis
Idiopathic pulmonary fibrosis (IPF), a fatal disease that is a result of complex interactions between genetics and the environment, has limited treatment options. We have identified the MUC5B promoter polymorphism and other common genetic variants that in aggregate explain roughly one-third of disea...
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Udgivet i: | Ann Am Thorac Soc |
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Main Authors: | , , , , |
Format: | Artigo |
Sprog: | Inglês |
Udgivet: |
American Thoracic Society
2015
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Fag: | |
Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4722833/ https://ncbi.nlm.nih.gov/pubmed/26595739 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1513/AnnalsATS.201503-110AW |
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