Case of Hereditary Papillary Renal Cell Carcinoma Type I in a Patient With a Germline MET Mutation in Russia

Hereditary papillary renal carcinoma (HPRC) is a rare autosomal dominant disease characterized by the development of multiple papillary type I renal cell carcinomas. This hereditary kidney cancer form is caused by activating mutations in MET. Descriptions of patients with HPRC are scarce in the worl...

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Detalles Bibliográficos
Autores principales: Mikhaylenko, Dmitry S., Klimov, Alexey V., Matveev, Vsevolod B., Samoylova, Svetlana I., Strelnikov, Vladimir V., Zaletaev, Dmitry V., Lubchenko, Ludmila N., Alekseev, Boris Y., Nemtsova, Marina V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Oncology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6985093/
https://www.ncbi.nlm.nih.gov/pubmed/32039030
http://dx.doi.org/10.3389/fonc.2019.01566

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6985093/
https://www.ncbi.nlm.nih.gov/pubmed/32039030
http://dx.doi.org/10.3389/fonc.2019.01566

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