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Ultra-rare RTEL1 gene variants associate with acute severity of COVID-19 and evolution to pulmonary fibrosis as a specific long COVID disorder.

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Bibliographic Details
Title: Ultra-rare RTEL1 gene variants associate with acute severity of COVID-19 and evolution to pulmonary fibrosis as a specific long COVID disorder.
Authors: Bergantini, Laura1 (AUTHOR), Baldassarri, Margherita2,3 (AUTHOR), d'Alessandro, Miriana1 (AUTHOR), Brunelli, Giulia2,3 (AUTHOR), Fabbri, Gaia1 (AUTHOR), Zguro, Kristina2,3 (AUTHOR), Degl'Innocenti, Andrea2,3 (AUTHOR), GEN-COVID Multicenter study (AUTHOR), Mari, Francesca (AUTHOR), Daga, Sergio (AUTHOR), Meloni, Ilaria (AUTHOR), Bruttini, Mirella (AUTHOR), Croci, Susanna (AUTHOR), Lista, Mirjam (AUTHOR), Maffeo, Debora (AUTHOR), Pasquinelli, Elena (AUTHOR), Serio, Viola Bianca (AUTHOR), Antolini, Enrica (AUTHOR), Basso, Simona Letizia (AUTHOR), Minetto, Samantha (AUTHOR)
Source: Respiratory Research. 6/17/2023, Vol. 24 Issue 1, p1-9. 9p.
Database: Academic Search Ultimate
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Description
ISSN:14659921
DOI:10.1186/s12931-023-02458-7