Identification of autosomal recessive novel genes and retinal phenotypes in members of the solute carrier (SLC) superfamily.

MLA

Millo, Talya, et al. “Identification of Autosomal Recessive Novel Genes and Retinal Phenotypes in Members of the Solute Carrier (SLC) Superfamily.” Genetics in Medicine : Official Journal of the American College of Medical Genetics, vol. 24, no. 7, July 2022, pp. 1523–35. EBSCOhost, https://doi.org/10.1016/j.gim.2022.03.020.

APA

Millo, T., Rivera, A., Obolensky, A., Marks-Ohana, D., Xu, M., Li, Y., Wilhelm, E., Gopalakrishnan, P., Gross, M., Rosin, B., Hanany, M., Webster, A., Tracewska, A. M., Koenekoop, R. K., Chen, R., Arno, G., Schueler-Furman, O., Roosing, S., Banin, E., & Sharon, D. (2022). Identification of autosomal recessive novel genes and retinal phenotypes in members of the solute carrier (SLC) superfamily. Genetics in Medicine : Official Journal of the American College of Medical Genetics, 24(7), 1523–1535. https://doi.org/10.1016/j.gim.2022.03.020

Chicago

Millo, Talya, Antonio Rivera, Alexey Obolensky, Devora Marks-Ohana, Mingchu Xu, Yumei Li, Enosh Wilhelm, et al. 2022. “Identification of Autosomal Recessive Novel Genes and Retinal Phenotypes in Members of the Solute Carrier (SLC) Superfamily.” Genetics in Medicine : Official Journal of the American College of Medical Genetics 24 (7): 1523–35. doi:10.1016/j.gim.2022.03.020.