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Idiopathic Pulmonary Fibrosis Is a Genetic Disease Involving Mucus and the Peripheral Airways

Idiopathic pulmonary fibrosis (IPF) is localized to the lung, is characterized by a pattern of heterogeneous, subpleural patches of fibrotic, remodeled lung, and is associated with a median survival of 3–5 years after diagnosis. A common gain-of-function MUC5B promoter variant, rs35705950, is the st...

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書目詳細資料
發表在:Ann Am Thorac Soc
主要作者: Schwartz, David A.
格式: Artigo
語言:Inglês
出版: American Thoracic Society 2018
主題:
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC6322034/
https://ncbi.nlm.nih.gov/pubmed/30431344
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1513/AnnalsATS.201802-144AW
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