APA (7th ed.) Citation

Has, C., & Haußer-Siller, I. (2017). Monoallelic large intragenic KRT5 deletions account for genetically unsolved cases of Epidermolysis bullosa simplex. The journal of investigative dermatology, 137(10), . https://doi.org/10.1016/j.jid.2017.05.016

Chicago Style (17th ed.) Citation

Has, Cristina, and Ingrid Haußer-Siller. "Monoallelic Large Intragenic KRT5 Deletions Account for Genetically Unsolved Cases of Epidermolysis Bullosa Simplex." The Journal of Investigative Dermatology 137, no. 10 (2017). https://doi.org/10.1016/j.jid.2017.05.016.

MLA (9th ed.) Citation

Has, Cristina, and Ingrid Haußer-Siller. "Monoallelic Large Intragenic KRT5 Deletions Account for Genetically Unsolved Cases of Epidermolysis Bullosa Simplex." The Journal of Investigative Dermatology, vol. 137, no. 10, 2017, https://doi.org/10.1016/j.jid.2017.05.016.