MUTYH ‐associated polyposis – colorectal phenotype and management
Author:
Affiliation:
1. Polyposis Registry St Mark’s Hospital Harrow UK
2. Department of Surgery and Cancer Imperial College London London UK
Publisher
Wiley
Subject
Gastroenterology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/codi.15078
Reference25 articles.
1. Inherited variants of MYH associated with somatic G:C→T:A mutations in colorectal tumors
2. Biallelic germline mutations in MYH predispose to multiple colorectal adenoma and somatic G:C->T:A mutations
3. Germline MutY Human Homologue Mutations and Colorectal Cancer: A Multisite Case-Control Study
4. Prevalence and Penetrance of Major Genes and Polygenes for Colorectal Cancer
5. Autosomal recessive colorectal adenomatous polyposis due to inherited mutations of MYH
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1. Hereditary Gastrointestinal Tumor Syndromes: When Risk Comes with Your Genes;Current Issues in Molecular Biology;2024-06-26
2. Phenotype correlations with pathogenic DNA variants in theMUTYHgene;2024-05-15
3. Updated European guidelines for clinical management of familial adenomatous polyposis (FAP), MUTYH-associated polyposis (MAP), gastric adenocarcinoma, proximal polyposis of the stomach (GAPPS) and other rare adenomatous polyposis syndromes: a joint EHTG-ESCP revision;British Journal of Surgery;2024-05
4. Low adenoma burden in unselected patients with a pathogenic APC variant;Genetics in Medicine;2023-12
5. Ergebnisse der endoskopischen Vorsorge und Therapie des Duodenums bei MUTYH-assoziierter Polyposis;Zentralblatt für Chirurgie - Zeitschrift für Allgemeine, Viszeral-, Thorax- und Gefäßchirurgie;2023-11-23
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