Checkpoint Kinase 2 (CHEK2) Mutation in Renal Cell Carcinoma: A Single-Center Experience

Renal cell carcinoma (RCC) occurs in sporadic and heritable forms. Genetic mutations have been identified as risk factors in 1–2% of RCC. The aim of this study was to evaluate I157T and CHEK2*1100delC mutations of checkpoint kinase 2 (CHEK2) gene in RCC. Medical records of 40 clear cell RCC patients...

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Detalles Bibliográficos
Autores principales: Huszno, Joanna, Kołosza, Zofia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Codon Publications 2018
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5906733/
https://www.ncbi.nlm.nih.gov/pubmed/29682443
http://dx.doi.org/10.15586/jkcvhl.2018.101

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5906733/
https://www.ncbi.nlm.nih.gov/pubmed/29682443
http://dx.doi.org/10.15586/jkcvhl.2018.101

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