Familial Lynch syndrome with early age of onset and confirmed splice site mutation in MSH2: A case report-Reference-Cited by-同舟云学术

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Familial Lynch syndrome with early age of onset and confirmed splice site mutation in MSH2: A case report

Published:2022-03-14 Issue:5 Volume:16 Page:
ISSN:2049-9434
Container-title:Biomedical Reports
language:
Short-container-title:Biomed Rep

Author:

Kamburova Zornitsa¹,Popovska Savelina²,Kovacheva Katya¹,Petrov Krasimir²,Nikolova Slavena¹

Affiliation:

1. Department of Medical Genetics, Medical University‑Pleven, Center of Medical Genetics in University Hospital ‘Dr. Georgi Stranski’, 5800 Pleven, Bulgaria

2. Department of Pathoanatomy, Medical University‑Pleven, University Hospital ‘Dr. Georgi Stranski’, 5800 Pleven, Bulgaria

Publisher

Spandidos Publications

Subject

General Pharmacology, Toxicology and Pharmaceutics,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

Reference35 articles.

1. Novel implications in molecular diagnosis of Lynch syndrome;Liccardo;Gastroenterol Res Pract,2017

2. A genomic portrait of human microsatellite variation;Payseur;Mol Biol Evol,2010

3. Recent discoveries in the molecular genetics of Lynch syndrome;Boland;Fam Cancer,2016

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Whole exome sequencing identifies MAP3K1, MSH2, and MLH1 as potential cancer‐predisposing genes in familial early‐onset colorectal cancer;The Kaohsiung Journal of Medical Sciences;2023-06-14

2. A Novel MSH6 Gene Variant in a Lynch Syndrome Patient with Lipomas;Clinics and Practice;2023-04-07

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