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Dive into the research topics of 'Exome sequencing links mutations in PARN and RTEL1 with familial pulmonary fibrosis and telomere shortening'. Together they form a unique fingerprint.- Sort by
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Bridget D. Stuart, Jungmin Choi, Samir Zaidi, Chao Xing, Brody Holohan, Rui Chen, Mihwa Choi, Pooja Dharwadkar, Fernando Torres, Carlos E. Girod, Jonathan Weissler, John Fitzgerald, Corey Kershaw, Julia Klesney-Tait, Yolanda Mageto, Jerry W. Shay, Weizhen Ji, Kaya Bilguvar, Shrikant Mane, Richard P. Lifton
Research output: Contribution to journal › Article › peer-review