Identification of Germline Mutations in Upper Tract Urothelial Carcinoma With Suspected Lynch Syndrome

OBJECTIVE: Whole-exon sequencing (WES) is a commercially available tool for hereditary disease testing. However, little is known about hereditary upper-tract urothelial carcinoma (UTUC) in the Chinese population. This study aims to investigate the prevalence of Lynch syndrome (LS) in UTUC patients w...

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Detalles Bibliográficos
Autores principales: Guan, Bao, Wang, Jie, Li, Xuesong, Lin, Lin, Fang, Dong, Kong, Wenwen, Tian, Chuangyu, Li, Juan, Yang, Kunlin, Han, Guanpeng, Wu, Yucai, He, Yuhui, Peng, Yiji, Yu, Yanfei, He, Qun, He, Shiming, Gong, Yanqing, Zhou, Liqun, Tang, Qi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Oncology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8966221/
https://www.ncbi.nlm.nih.gov/pubmed/35372080
http://dx.doi.org/10.3389/fonc.2022.774202

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8966221/
https://www.ncbi.nlm.nih.gov/pubmed/35372080
http://dx.doi.org/10.3389/fonc.2022.774202

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