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Structural Variants in Severe COVID-19: Clinical Impact Assessment

Background: Several genes and genomic regions have been implicated in COVID-19 susceptibility and severity, but their clinical relevance remains uncertain. We comprehensively assessed both copy number variants (CNVs) and single-nucleotide variants (SNVs) disrupting genes implicated in COVID-19 in a...

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Sábháilte in:
Príomhchruthaitheoirí: Johanna Kämpe, Jesper Eisfeldt, Per Nordberg, Agneta Nordenskjöld, Magnus Nordenskjöld, Miklos Lipcsey, Michael Marks-Hultström, Robert Frithiof, Jonathan Grip, Olav Rooijackers, Hugo Zeberg, Anders Kämpe
Formáid: Artigo
Teanga:Inglês
Foilsithe / Cruthaithe: MDPI AG 2026-01-01
Sraith:COVID
Ábhair:
COVID-19 severity
copy number variants (CNVs)
single nucleotide variants (SNVs)
intensive care patients
whole exome sequencing (WES)
phenotype data
Rochtain ar líne:https://www.mdpi.com/2673-8112/6/1/10
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