Cita APA (7a ed.)

X, H., T, H., Y, L., L, Z., L, Z., X, P., & S, Z. (2021). Identification of a Novel VPS13B Mutation in a Chinese Patient with Cohen Syndrome by Whole-Exome Sequencing. Dove Medical Press.

Cita Chicago Style (17a ed.)

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

Cita MLA (8a ed.)

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