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

Authors

  1. Correspondence to Dr Khawla S Al-Kuraya, Human Cancer Genomic Research, King Faisal Specialist Hospital and Research Center, Riyadh 11431, Saudi Arabia; kkuraya{at}kfshrc.edu.sa
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Citation

Siraj AK, Masoodi T, Bu R, et al
The study of Lynch syndrome in a special population reveals a strong founder effect and an unusual mutational mechanism in familial adenomatous polyposis

Publication history

  • Received December 19, 2019
  • Revised January 6, 2020
  • Accepted January 6, 2020
  • First published January 10, 2020.
Online issue publication 
October 07, 2020

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