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Candidate genes of idiopathic pulmonary fibrosis: current evidence and research
Idiopathic pulmonary fibrosis (IPF) is a group of common and lethal forms of idiopathic interstitial pulmonary disease. IPF is characterized by a progressive decline in lung function with a median survival of 2–3 years after diagnosis. Although the pathogenesis of the disease remains unknown, geneti...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Dove Medical Press
2016
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4745857/ https://www.ncbi.nlm.nih.gov/pubmed/26893575 http://dx.doi.org/10.2147/TACG.S61999 |