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Front Oncol. 2020 Jan 21;9:1566. doi: 10.3389/fonc.2019.01566. eCollection 2019.

Case of Hereditary Papillary Renal Cell Carcinoma Type I in a Patient With a Germline .

Frontiers in oncology

Dmitry S Mikhaylenko, Alexey V Klimov, Vsevolod B Matveev, Svetlana I Samoylova, Vladimir V Strelnikov, Dmitry V Zaletaev, Ludmila N Lubchenko, Boris Y Alekseev, Marina V Nemtsova

Affiliations

  1. Laboratory of Medical Genetics, Institute of Molecular Medicine, Scientific Biotechnological Park of Biomedicine, Sechenov University, Moscow, Russia.
  2. Laboratory of Pathology and Molecular Genetics, N. Lopatkin Institute of Urology and Interventional Radiology - Branch of the National Medical Research Center of Radiology, Moscow, Russia.
  3. Laboratory of Epigenetics, Research Centre for Medical Genetics Named After Academician N. P. Bochkov, Moscow, Russia.
  4. Department of Urology, Institute of Clinical Oncology, N. N. Blokhin National Medical Research Center of Oncology, Moscow, Russia.

PMID: 32039030 PMCID: PMC6985093 DOI: 10.3389/fonc.2019.01566

Abstract

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

Copyright © 2020 Mikhaylenko, Klimov, Matveev, Samoylova, Strelnikov, Zaletaev, Lubchenko, Alekseev and Nemtsova.

Keywords: MET gene; germline mutation; hereditary cancer syndrome; kidney cancer; papillary renal cell carcinoma

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