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...

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Detalles Bibliográficos
Autores principales: Sobocińska, Joanna, Kolenda, Tomasz, Teresiak, Anna, Badziąg-Leśniak, Natalia, Kopczyńska, Magda, Guglas, Kacper, Przybyła, Anna, Filas, Violetta, Bogajewska-Ryłko, Elżbieta, Lamperska, Katarzyna, Mackiewicz, Andrzej
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7600989/
https://www.ncbi.nlm.nih.gov/pubmed/33027913
http://dx.doi.org/10.3390/diagnostics10100786

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7600989/
https://www.ncbi.nlm.nih.gov/pubmed/33027913
http://dx.doi.org/10.3390/diagnostics10100786

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