Lynch syndrome and Muir-Torre phenotype associated with a recurrent variant in the 3’UTR of the MSH6 gene

Author:

Cini Giulia,Carnevali Ileana,Sahnane Nora,Chiaravalli Anna Maria,Dell'Elice Anastasia,Maestro Roberta,Pin ElisaORCID,Bestetti IlariaORCID,Radovic SlobodankaORCID,Armelao Franco,Viel Alessandra,Tibiletti Maria Grazia

Publisher

Elsevier BV

Subject

Cancer Research,Genetics,Molecular Biology

Reference29 articles.

1. Milestones of Lynch syndrome: 1895–2015;Lynch;Nat Rev Cancer,2015

2. Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database;Dominguez-Valentin;Genet Med,2019

3. The biochemical basis of microsatellite instability and abnormal immunohistochemistry and clinical behavior in Lynch Syndrome: from bench to bedside;Boland;Fam Cancer,2008

4. Immunohistochemistry identifies carriers of mismatch repair gene defects causing hereditary nonpolyposis colorectal cancer;Stormorken;J Clin Oncol,2005

5. Gene variants of unknown clinical significance in Lynch syndrome. An introduction for clinicians;Sijmons;Fam Cancer,2013

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