A novel low-risk germline variant in the SH2 domain of the SRC gene affects multiple pathways in familial colorectal cancer

Colorectal cancer (CRC) shows one of the largest proportions of familial cases among different malignancies, but only 5-10% of all CRC cases are linked to mutations in established predisposition genes. Thus, familial CRC constitutes a promising target for the identification of novel, high- to modera...

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Main Authors: Skopelitou, Diamanto (Author) , Miao, Beiping (Author) , Srivastava, Aayushi (Author) , Kumar, Abhishek (Author) , Kuświk, Magdalena (Author) , Dymerska, Dagmara (Author) , Paramasivam, Nagarajan (Author) , Schlesner, Matthias (Author) , Lubiński, Jan (Author) , Hemminki, Kari (Author) , Försti, Asta (Author) , Bandapalli, Obul Reddy (Author)
Format: Article (Journal)
Language:English
Published: 1 April 2021
In: Journal of Personalized Medicine
Year: 2021, Volume: 11, Issue: 4, Pages: 1-15
ISSN:2075-4426
DOI:10.3390/jpm11040262
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.3390/jpm11040262
Verlag, lizenzpflichtig, Volltext: https://www.mdpi.com/2075-4426/11/4/262
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Author Notes:Diamanto Skopelitou, Beiping Miao, Aayushi Srivastava, Abhishek Kumar, Magdalena Kuświk, Dagmara Dymerska, Nagarajan Paramasivam, Matthias Schlesner, Jan Lubiński, Kari Hemminki, Asta Försti, Obul Reddy Bandapalli
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