Autosomal dominant monilethrix with incomplete penetrance due to a novel KRT86 mutation in a Chinese family.

MLA

Dai, Ru, et al. “Autosomal Dominant Monilethrix with Incomplete Penetrance Due to a Novel KRT86 Mutation in a Chinese Family.” Anais Brasileiros de Dermatologia, vol. 99, no. 4, July 2024, pp. 606–09. EBSCOhost, https://doi.org/10.1016/j.abd.2022.12.010.

APA

Dai, R., Wang, T., & Wu, X. (2024). Autosomal dominant monilethrix with incomplete penetrance due to a novel KRT86 mutation in a Chinese family. Anais Brasileiros de Dermatologia, 99(4), 606–609. https://doi.org/10.1016/j.abd.2022.12.010

Chicago

Dai, Ru, Tingting Wang, and Xianjie Wu. 2024. “Autosomal Dominant Monilethrix with Incomplete Penetrance Due to a Novel KRT86 Mutation in a Chinese Family.” Anais Brasileiros de Dermatologia 99 (4): 606–9. doi:10.1016/j.abd.2022.12.010.