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• W2080774991 abstract "RCC represents a group of clinically and genetically diverse diseases. Familial RCC syndromes, although rare, provide an invaluable model to study the molecular mechanisms of renal carcinogenesis. Many causative oncogenes and tumor suppressor genes have been identified and it is now possible to identify the affected individuals and carriers by genetic testing. Understanding of the molecular pathways of these genes will have a significant impact on the diagnosis and treatment of familial and sporadic RCC." @default.
• W2080774991 created "2016-06-24" @default.
• W2080774991 creator A5022480456 @default.
• W2080774991 creator A5064373607 @default.
• W2080774991 date "2005-06-01" @default.
• W2080774991 modified "2023-09-27" @default.
• W2080774991 title "Molecular Genetics of Familial Renal Cell Carcinoma Syndromes" @default.
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• W2080774991 doi "https://doi.org/10.1016/j.cll.2005.01.003" @default.
• W2080774991 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/15848736" @default.
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