Mimicking Behçet’s disease: GM‐CSF gain of function mutation in a family suffering from a Behçet’s disease‐like disorder marked by extreme pathergy
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A. Hoischen | L. Joosten | M. Netea | P. Arts | D. Lefeber | R. Silvestre | F. L. van de Veerdonk | T. Mantere | Xiaowen Wang | B. Rösler | B. Heinhuis