Identification of Lynch Syndrome in Patients with Endometrial Cancer Based on a Germline Next Generation Sequencing Multigene Panel Test

SIMPLE SUMMARY: Lynch Syndrome (LS) is a hereditary cancer syndrome caused by an autosomal dominant mutation in one of the DNA mismatch repair (MMR) genes. Understanding the clinical traits of endometrial cancer, which is one of the most frequent as well as the earliest diagnosed cancer types of LS-...

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Detalles Bibliográficos
Autores principales: Kim, Yoo-Na, Kim, Min Kyu, Lee, Young Joo, Lee, Youngeun, Sohn, Ji Yeon, Lee, Jung-Yun, Choi, Min Chul, Kim, Migang, Jung, Sang Geun, Joo, Won Duk, Lee, Chan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9316192/
https://www.ncbi.nlm.nih.gov/pubmed/35884469
http://dx.doi.org/10.3390/cancers14143406

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9316192/
https://www.ncbi.nlm.nih.gov/pubmed/35884469
http://dx.doi.org/10.3390/cancers14143406

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