Structural modeling of a novel SLC38A8 mutation that causes foveal hypoplasia.

MLA

Toral, Marcus A., et al. “Structural Modeling of a Novel SLC38A8 Mutation That Causes Foveal Hypoplasia.” Molecular Genetics & Genomic Medicine, vol. 5, no. 3, Feb. 2017, pp. 202–09. EBSCOhost, https://doi.org/10.1002/mgg3.266.

APA

Toral, M. A., Velez, G., Boudreault, K., Schaefer, K. A., Xu, Y., Saffra, N., Bassuk, A. G., Tsang, S. H., & Mahajan, V. B. (2017). Structural modeling of a novel SLC38A8 mutation that causes foveal hypoplasia. Molecular Genetics & Genomic Medicine, 5(3), 202–209. https://doi.org/10.1002/mgg3.266

Chicago

Toral, Marcus A, Gabriel Velez, Katherine Boudreault, Kellie A Schaefer, Yu Xu, Norman Saffra, Alexander G Bassuk, Stephen H Tsang, and Vinit B Mahajan. 2017. “Structural Modeling of a Novel SLC38A8 Mutation That Causes Foveal Hypoplasia.” Molecular Genetics & Genomic Medicine 5 (3): 202–9. doi:10.1002/mgg3.266.