Lynch Syndrome-Related Clear Cell Carcinoma of the Cervix: A Case Report

Lynch syndrome, a hereditary cancer syndrome, occurs because of germline mutations in at least one of four DNA mismatch repair genes (MutL Homolog 1 (MLH1), MutS Homolog 2 (MSH2), MutS Homolog 6 (MSH6), and PMS1 Homolog 2 (PMS2)). The disorder is associated with colorectal, endometrial, and other ep...

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Detalles Bibliográficos
Autores principales: Nakamura, Kohei, Nakayama, Kentaro, Minamoto, Toshiko, Ishibashi, Tomoka, Ohnishi, Kaori, Yamashita, Hitomi, Ono, Ruriko, Sasamori, Hiroki, Razia, Sultana, Hossain, Mohammad Mahmud, Kamrunnahar, Shanta, Ishikawa, Masako, Ishikawa, Noriyoshi, Kyo, Satoru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5979360/
https://www.ncbi.nlm.nih.gov/pubmed/29587389
http://dx.doi.org/10.3390/ijms19040979

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5979360/
https://www.ncbi.nlm.nih.gov/pubmed/29587389
http://dx.doi.org/10.3390/ijms19040979

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