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    A loss‐of‐function <scp><i>NCSTN</i></scp> mutation associated with familial <scp>Dowling Degos disease</scp> and hidradenitis suppurativa

    A loss‐of‐function <scp><i>NCSTN</i></scp> mutation associated with familial <scp>Dowling Degos disease</scp> and hidradenitis suppurativa 由 Ana Sofia Lima Estevão de Oliveira, Roberta Cardoso de Siqueira, Cécile Nait‐Meddour, Paola Maura Tricarico, Ronald Moura, Almerinda Agrelli, Pio D’Adamo, Stéphane Jamain, Sérgio Crovella, Maria de Fátima Medeiros Brito, Michele Boniotto, Lucas André Cavalcanti Brandão

    出版 2023
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