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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Vydáno v:Cancer Genomics Proteomics
Hlavní autoři: 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
Médium: Artigo
Jazyk:Inglês
Vydáno: International Institute of Anticancer Research 2021
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Research Article
On-line přístup: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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