Clinical Utility of Functional RNA Analysis for the Reclassification of Splicing Gene Variants in Hereditary Cancer

Background: Classification of splicing variants (SVs) in genes associated with hereditary cancer is often challenging. The aim of this study was to investigate the occurrence of SVs in hereditary cancer genes and the clinical utility of RNA analysis. Material and Methods: 1518 individuals were teste...

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Opis bibliograficzny
Wydane w:Cancer Genomics Proteomics
Główni autorzy: AGIANNITOPOULOS, KONSTANTINOS, PEPE, GEORGIA, PAPADOPOULOU, EIRINI, TSAOUSIS, GEORGIOS N., KAMPOURI, STAVROULA, MARAVELAKI, SONIA, FASSAS, ATHANASSIOS, CHRISTODOULOU, CHRISTOS, IOSIFIDOU, RODONIKI, KARAGEORGOPOULOU, SOFIA, MARKOPOULOS, CHRISTOS, NATSIOPOULOS, IOANNIS, PAPAZISIS, KONSTANTINOS, VASILAKI-ANTONATOU, MARIA, VENIZELOS, VASSILEIOS, OZMEN, VAHIT, TANSAN, SUALP, KABAN, KERIM, ENIU, DAN TUDOR, CHIOREAN, ANGELICA, NASIOULAS, GEORGE
Format: Artigo
Język:Inglês
Wydane: International Institute of Anticancer Research 2021
Hasła przedmiotowe:
Research Article
Dostęp online:https://ncbi.nlm.nih.gov/pmc/articles/PMC8126331/
https://ncbi.nlm.nih.gov/pubmed/33893081
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.21873/cgp.20259
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