A loss‐of‐function <scp> <i>NCSTN</i> </scp> mutation associated with familial <scp>Dowling Degos disease</scp> and hidradenitis suppurativa
Ana Sofia Lima Estevão de Oliveira(Universidade Federal de Pernambuco), Lucas André Cavalcanti Brandão(Universidade Federal de Pernambuco)
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