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    Article

    Mutation of the proline P81 into a serine modifies the tumour suppressor function of the von Hippel–Lindau gene in the ccRCC

    The von Hippel–Lindau disease is an autosomal dominant syndrome associated with tumour formation in various tissues, such as retina, central nervous system, kidney, and adrenal glands. VHL gene deletion or mut...

    Franck Chesnel, Emmanuelle Jullion, Olivier Delalande… in British Journal of Cancer (2022)