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    Open Access

    Multi-omics analyses of MEN1 missense mutations identify disruption of menin–MLL and menin–JunD interactions as critical requirements for molecular pathogenicity

    Loss-of-function mutations of the multiple endocrine neoplasia type 1 (MEN1) gene are causal to the MEN1 tumor syndrome, but they are also commonly found in sporadic pancreatic neuroendocrine tumors and other typ...

    Koen M. A. Dreijerink, Ezgi Ozyerli-Goknar, Stefanie Koidl… in Epigenetics & Chromatin (2022)

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