New kinase‐deficient PAK2 variants associated with Knobloch syndrome type 2.

MLA

Schnur, Rhonda E., et al. “New Kinase‐deficient PAK2 Variants Associated with Knobloch Syndrome Type 2.” Clinical Genetics, vol. 106, no. 4, Oct. 2024, pp. 518–24. EBSCOhost, https://doi.org/10.1111/cge.14578.

APA

Schnur, R. E., Dvořáček, L., Kalsner, L., Shapiro, F. L., Grebeňová, D., Yanni, D., Wasserman, B. N., Agrawal, P., Parker, M., Yu, T., Douglas, J., Young, V., D’Gama, A., Hills, S., Wojcik, M., Brownstein, C., Genetti, C., Schmith, A. K., Dyer, L. M., & Antonarakis, S. E. (2024). New kinase‐deficient PAK2 variants associated with Knobloch syndrome type 2. Clinical Genetics, 106(4), 518–524. https://doi.org/10.1111/cge.14578

Chicago

Schnur, Rhonda E., Lukáš Dvořáček, Louisa Kalsner, Faye L. Shapiro, Dana Grebeňová, Diana Yanni, Barry N. Wasserman, et al. 2024. “New Kinase‐deficient PAK2 Variants Associated with Knobloch Syndrome Type 2.” Clinical Genetics 106 (4): 518–24. doi:10.1111/cge.14578.