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...

詳細記述

保存先:
書誌詳細
出版年:Cancer Genomics Proteomics
主要な著者: 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
フォーマット: Artigo
言語:Inglês
出版事項: International Institute of Anticancer Research 2021
主題:
Research Article
オンライン･アクセス: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
タグ: タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!

類似資料