The study of Lynch syndrome in a special population reveals a strong founder effect and an unusual mutational mechanism in familial adenomatous polyposis.

Content Provider	Europe PMC
Author	Siraj, Abdul K Masoodi, Tariq Bu, Rong Parvathareddy, Sandeep Kumar Siraj, Sarah Alassiri, Ali Al-Dayel, Fouad Alkuraya, Fowzan S Al-Kuraya, Khawla S
Copyright Year	2020
ISSN	00175749
Journal	Gut
Volume Number	69
PubMed Central reference number	PMC7569390
Issue Number	11
PubMed reference number	31924657
e-ISSN	14683288
DOI	10.1136/gutjnl-2019-320511
Language	English
Publisher	BMJ
Publisher Date	2020-01-10
Publisher Place	BMA House, Tavistock Square, London, WC1H 9JR
Access Restriction	Open
Rights License	This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/. © Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.
Subject Keyword	colorectal cancer familial adenomatous polyposis HNPCC syndrome
Content Type	Text
Resource Type	Article
Subject	Gastroenterology