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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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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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  Data: 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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  Data: <searchLink fieldCode="JN" term="%22Respiratory+Research%22">Respiratory Research</searchLink>. 6/17/2023, Vol. 24 Issue 1, p1-9. 9p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=164370158
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              Text: 6/17/2023
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