Diagnostics of Mutations in MMR/EPCAM Genes and Their Role in the Treatment and Care of Patients with Lynch Syndrome

Lynch syndrome (LS), also known as hereditary nonpolyposis colorectal cancer (HNPCC), is a disorder caused by an autosomal dominant heterozygous germline mutation in one of the DNA mismatch repair (MMR) genes. Individuals with LS are at an increased risk of developing colorectal and extracolonic can...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Diagnostics (Basel)
Prif Awduron: Sobocińska, Joanna, Kolenda, Tomasz, Teresiak, Anna, Badziąg-Leśniak, Natalia, Kopczyńska, Magda, Guglas, Kacper, Przybyła, Anna, Filas, Violetta, Bogajewska-Ryłko, Elżbieta, Lamperska, Katarzyna, Mackiewicz, Andrzej
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: MDPI 2020
Pynciau:
Review
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC7600989/
https://ncbi.nlm.nih.gov/pubmed/33027913
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/diagnostics10100786
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