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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Publicat a:Cancer Genomics Proteomics
Autors principals: 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
Idioma:Inglês
Publicat: International Institute of Anticancer Research 2021
Matèries:
Research Article
Accés en línia: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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