Insights from human genetic studies of lung and organ fibrosis
Author:
Publisher
American Society for Clinical Investigation
Subject
General Medicine
Link
https://www.jci.org/articles/view/93556/files/pdf
Reference131 articles.
1. Analysis of protein-coding genetic variation in 60,706 humans
2. Idiopathic pulmonary fibrosis
3. Exome sequencing links mutations in PARN and RTEL1 with familial pulmonary fibrosis and telomere shortening
4. An Exome Sequencing Study to Assess the Role of Rare Genetic Variation in Pulmonary Fibrosis
5. Dyskeratosis congenita in all its forms
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