IndraLab

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VHL binds PBRM1, BAP1, SETD2, and KDM5C. 2 / 2

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"The objective of this hypotheses-generating Radiogenomics study was to investigate associations between CT features of ccRCC and mutations of the genes VHL, PBRM1, SETD2, KDM5C , and BAP1."

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"The identification of genetic mutations is clinically relevant because both an advanced stage and poor survival have been associated with VHL, PBRM1, BAP1, SETD2, and KDM5C mutations [ xref , xref – xref ]."

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IndraLab

Statements

VHL binds PBRM1, BAP1, SETD2, and KDM5C. 2 / 2

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