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...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
में प्रकाशित:Cancer Genomics Proteomics
मुख्य लेखकों: 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
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: International Institute of Anticancer Research 2021
विषय:
Research Article
ऑनलाइन पहुंच: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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