APA (7th ed.) Citation

Bchetnia, M., Allard, J., Boucher‐Lafleur, A., Cruz Marino, T., Dupéré, A., Powell, J., . . . Laprise, C. (2020). Severe epidermolysis bullosa simplex phenotype caused by codominant mutations p.Ile377Thr in keratin 14 and p.Gly138Glu in keratin 5. Experimental Dermatology, 29(10), 961. https://doi.org/10.1111/exd.14189

Chicago Style (17th ed.) Citation

Bchetnia, Mbarka, Jean‐Pascal Allard, Anne‐Marie Boucher‐Lafleur, Tania Cruz Marino, Audrey Dupéré, Julie Powell, Catherine McCuaig, Marie‐Ève Bernier, and Catherine Laprise. "Severe Epidermolysis Bullosa Simplex Phenotype Caused by Codominant Mutations P.Ile377Thr in Keratin 14 and P.Gly138Glu in Keratin 5." Experimental Dermatology 29, no. 10 (2020): 961. https://doi.org/10.1111/exd.14189.

MLA (9th ed.) Citation

Bchetnia, Mbarka, et al. "Severe Epidermolysis Bullosa Simplex Phenotype Caused by Codominant Mutations P.Ile377Thr in Keratin 14 and P.Gly138Glu in Keratin 5." Experimental Dermatology, vol. 29, no. 10, 2020, p. 961, https://doi.org/10.1111/exd.14189.