Rare frameshift mutation in SERPINA3 contributes to generalized pustular psoriasis

Hüffmeier U, Sticht H, Wenzel J, Wilsmann-Theis D, Wolff K, Löhr S, Frey B, Hahn M, Ekici AB, Uebe S, Thiel C, Wiesmann da Silva Reis A, Prinz J, Oji V, Schulz P, Kingo K, Koks S, Moessner R, Munoz LE, Kremer A, Frey S (2019)

Publication Type: Conference contribution

Publication year: 2019

Journal

European Journal of Human Genetics Nature Publishing Group: Open Access Hybrid Model Option B

Publisher: NATURE PUBLISHING GROUP

City/Town: LONDON

Pages Range: 1366-1367

Conference Proceedings Title: EUROPEAN JOURNAL OF HUMAN GENETICS

Event location: Gothenburg, SWEDEN

Authors with CRIS profile

Ulrike Hüffmeier Medizinische Fakultät Heinrich Sticht Professur für Bioinformatik Sabine Löhr Lehrstuhl für Humangenetik Benjamin Frey Department of Radiation Oncology Arif Bülent Ekici Institute of Human Genetics Christian Thiel Medizinische Fakultät André Wiesmann da Silva Reis Lehrstuhl für Humangenetik Luis Munoz Becerra Department of Medicine 3 – Rheumatology and Immunology Andreas Kremer Department of Medicine 1 – Gastroenterology, Pneumology and Endocrinology Silke Frey Department of Medicine 3 – Rheumatology and Immunology

Involved external institutions

Ludwig-Maximilians-Universität (LMU) DE Germany (DE) Rheinische Friedrich-Wilhelms-Universität Bonn DE Germany (DE) Westfälische Wilhelms-Universität (WWU) Münster DE Germany (DE) University of Tartu EE Estonia (EE) Fachklinik Bad Bentheim DE Germany (DE) Georg-August-Universität Göttingen DE Germany (DE)

How to cite

APA:

Hüffmeier, U., Sticht, H., Wenzel, J., Wilsmann-Theis, D., Wolff, K., Löhr, S.,... Frey, S. (2019). Rare frameshift mutation in SERPINA3 contributes to generalized pustular psoriasis. In EUROPEAN JOURNAL OF HUMAN GENETICS (pp. 1366-1367). Gothenburg, SWEDEN: LONDON: NATURE PUBLISHING GROUP.

MLA:

Hüffmeier, Ulrike, et al. "Rare frameshift mutation in SERPINA3 contributes to generalized pustular psoriasis." Proceedings of the 52nd Conference of the European-Society-of-Human-Genetics (ESHG), Gothenburg, SWEDEN LONDON: NATURE PUBLISHING GROUP, 2019. 1366-1367.

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