PDCD1 and IFNL4 genetic variants and risk of developing hepatitis C virus‐related diseases

BACKGROUND: Genetic variants of IFNL4 and PDCD1 genes have been shown to influence the spontaneous clearance of hepatitis C virus (HCV) infection. We investigated the IFNL4 rs12979860 and the PDCD1 polymorphisms in 734 HCV‐positive patients, including 461 cases with liver disease of varying severity...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Liver Int
Päätekijät: De Re, Valli, Tornesello, Maria Lina, De Zorzi, Mariangela, Caggiari, Laura, Pezzuto, Francesca, Leone, Patrizia, Racanelli, Vito, Lauletta, Gianfranco, Zanussi, Stefania, Repetto, Ombretta, Gragnani, Laura, Rossi, Francesca Maria, Dolcetti, Riccardo, Zignego, Anna Linda, Buonaguro, Franco M., Steffan, Agostino
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: John Wiley and Sons Inc. 2020
Aiheet:
Genetics and Rare Liver Diseases
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC7839592/
https://ncbi.nlm.nih.gov/pubmed/32937024
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/liv.14667
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