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Rare Variants in <i>RTEL1</i> Are Associated with Familial Interstitial Pneumonia

196

Citations

37

References

2015

Year

Abstract

Rare loss-of-function variants in RTEL1 represent a newly defined genetic predisposition for FIP, supporting the importance of telomere-related pathways in pulmonary fibrosis.

References

YearCitations

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