A novel insertion mutation of CDSN responsible for hypotrichosis simplex of scalp in a Chinese family.

MLA

Huang, H., et al. “A Novel Insertion Mutation of CDSN Responsible for Hypotrichosis Simplex of Scalp in a Chinese Family.” Clinical and Experimental Dermatology, vol. 43, no. 6, Aug. 2018, pp. 722–23. EBSCOhost, https://doi.org/10.1111/ced.13547.

APA

Huang, H., Sun, J., Fu, L., Wu, J., Guo, H., Yang, C., Zheng, X., Tang, H., Sun, L., & Zhang, X. (2018). A novel insertion mutation of CDSN responsible for hypotrichosis simplex of scalp in a Chinese family. Clinical and Experimental Dermatology, 43(6), 722–723. https://doi.org/10.1111/ced.13547

Chicago

Huang, H, J Sun, L Fu, J Wu, H Guo, C Yang, X Zheng, H Tang, L Sun, and X Zhang. 2018. “A Novel Insertion Mutation of CDSN Responsible for Hypotrichosis Simplex of Scalp in a Chinese Family.” Clinical and Experimental Dermatology 43 (6): 722–23. doi:10.1111/ced.13547.