Cite
Phenotypic suppression of acral peeling skin syndrome in a patient with autosomal recessive congenital ichthyosis.
MLA
Mohamad, Janan, et al. “Phenotypic Suppression of Acral Peeling Skin Syndrome in a Patient with Autosomal Recessive Congenital Ichthyosis.” Experimental Dermatology, vol. 29, no. 8, Aug. 2020, pp. 742–48. EBSCOhost, https://doi.org/10.1111/exd.14140.
APA
Mohamad, J., Nanda, A., Pavlovsky, M., Peled, A., Malchin, N., Malovitski, K., Pramanik, R., Weissglas, V. D., Shomron, N., McGrath, J., Sprecher, E., & Sarig, O. (2020). Phenotypic suppression of acral peeling skin syndrome in a patient with autosomal recessive congenital ichthyosis. Experimental Dermatology, 29(8), 742–748. https://doi.org/10.1111/exd.14140
Chicago
Mohamad, Janan, Arti Nanda, Mor Pavlovsky, Alon Peled, Natalia Malchin, Kiril Malovitski, Rashida Pramanik, et al. 2020. “Phenotypic Suppression of Acral Peeling Skin Syndrome in a Patient with Autosomal Recessive Congenital Ichthyosis.” Experimental Dermatology 29 (8): 742–48. doi:10.1111/exd.14140.