Loss-of-function mutations in the filaggrin gene and alopecia areata: strong risk factor for a severe course of disease in patients comorbid for atopic disease.
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M. Nöthen | T. Wienker | A. Hillmer | R. Kruse | R. Betz | C. Schmael | T. Tüting | J. Pforr | B. Blaumeiser | A. Flaquer | S. Hanneken | S. Redler | J. Lambert | G. Lutz | S. Eigelshoven | J. De Weert | Anne-Katrin Kortüm