APA (7th ed.) Citation

Bernadett Kurz, M., Kevin-Thomas Koschitzki, M., Ute Hehr, M., Ute Germer, M., Julia Schreml, M., Florian Langhammer, M., & Stephan Schreml, M. (2023). Congenital ichthyosiform erythroderma with epidermolysis due to a novel frameshift mutation in KRT10. Elsevier.

Chicago Style (17th ed.) Citation

Bernadett Kurz, MD, MD Kevin-Thomas Koschitzki, MD Ute Hehr, MD Ute Germer, MD Julia Schreml, MD Florian Langhammer, and MD Stephan Schreml. Congenital Ichthyosiform Erythroderma with Epidermolysis Due to a Novel Frameshift Mutation in KRT10. Elsevier, 2023.

MLA (9th ed.) Citation

Bernadett Kurz, MD, et al. Congenital Ichthyosiform Erythroderma with Epidermolysis Due to a Novel Frameshift Mutation in KRT10. Elsevier, 2023.