APA

Betz R. C., Pforr J., Flaquer A., Redler S., Hanneken S., Eigelshoven S., Kortüm A., Tüting T., Lambert J., De Weert J., Hillmer A. M., Schmael C., Wienker T. F., Kruse R., Lutz G., Blaumeiser B. & Nöthen M. M. (20071029). 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. : The Journal of investigative dermatology.

Chicago

Betz Regina C, Pforr Jana, Flaquer Antonia, Redler Silke, Hanneken Sandra, Eigelshoven Sibylle, Kortüm Anne-Katrin, Tüting Thomas, Lambert Julien, De Weert Jozef, Hillmer Axel M, Schmael Christine, Wienker Thomas F, Kruse Roland, Lutz Gerhard, Blaumeiser Bettina and Nöthen Markus M. 20071029. 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. : The Journal of investigative dermatology.

Harvard

Betz R. C., Pforr J., Flaquer A., Redler S., Hanneken S., Eigelshoven S., Kortüm A., Tüting T., Lambert J., De Weert J., Hillmer A. M., Schmael C., Wienker T. F., Kruse R., Lutz G., Blaumeiser B. and Nöthen M. M. (20071029). 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. : The Journal of investigative dermatology.

MLA

Betz Regina C, Pforr Jana, Flaquer Antonia, Redler Silke, Hanneken Sandra, Eigelshoven Sibylle, Kortüm Anne-Katrin, Tüting Thomas, Lambert Julien, De Weert Jozef, Hillmer Axel M, Schmael Christine, Wienker Thomas F, Kruse Roland, Lutz Gerhard, Blaumeiser Bettina and Nöthen Markus M. 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. : The Journal of investigative dermatology. 20071029.