Homozygous Biallelic KRT5 Mutations in Epidermolysis Bullosa Simplex, Including a Complete Human Keratin 5 "Knock-Out", in Families with Extensive Consanguinity

Vahidnezhad H, Youssefian L, Daneshpazhooh M, Mahmoudi H, Kariminejad A, Fischer J, Christiansen J, Schneider H, Guy A, Liu L, Mcgrath JA, Has C, Uitto J (2019)


Publication Type: Conference contribution

Publication year: 2019

Journal

Publisher: ELSEVIER SCIENCE INC

City/Town: NEW YORK

Pages Range: S267-S267

Conference Proceedings Title: JOURNAL OF INVESTIGATIVE DERMATOLOGY

Event location: Bordeaux, FRANCE

DOI: 10.1016/j.jid.2019.07.308

Authors with CRIS profile

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How to cite

APA:

Vahidnezhad, H., Youssefian, L., Daneshpazhooh, M., Mahmoudi, H., Kariminejad, A., Fischer, J.,... Uitto, J. (2019). Homozygous Biallelic KRT5 Mutations in Epidermolysis Bullosa Simplex, Including a Complete Human Keratin 5 "Knock-Out", in Families with Extensive Consanguinity. In JOURNAL OF INVESTIGATIVE DERMATOLOGY (pp. S267-S267). Bordeaux, FRANCE: NEW YORK: ELSEVIER SCIENCE INC.

MLA:

Vahidnezhad, H., et al. "Homozygous Biallelic KRT5 Mutations in Epidermolysis Bullosa Simplex, Including a Complete Human Keratin 5 "Knock-Out", in Families with Extensive Consanguinity." Proceedings of the 49th Annual Meeting of the European-Society-for-Dermatological-Research (ESDR), Bordeaux, FRANCE NEW YORK: ELSEVIER SCIENCE INC, 2019. S267-S267.

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