APA (7th ed.) Citation

Hu X, Huang T, Liu Y, Zhang L, Zhu L, Peng X, & Zhang S. (2021). Identification of a Novel VPS13B Mutation in a Chinese Patient with Cohen Syndrome by Whole-Exome Sequencing. Dove Medical Press.

Chicago Style (17th ed.) Citation

Hu X, Huang T, Liu Y, Zhang L, Zhu L, Peng X, and Zhang S. Identification of a Novel VPS13B Mutation in a Chinese Patient with Cohen Syndrome by Whole-Exome Sequencing. Dove Medical Press, 2021.

MLA (9th ed.) Citation

Hu X, et al. Identification of a Novel VPS13B Mutation in a Chinese Patient with Cohen Syndrome by Whole-Exome Sequencing. Dove Medical Press, 2021.