APA (7th ed.) Citation

FC, R., G, T., S, C., G, C., S, W., I, M., . . . M, T. (2026). Loss of function of retinol dehydrogenase 11 causes a recessive syndrome characterized by myopathy, retinal dystrophy, juvenile cataracts, and microcephaly. Genetics in medicine : official journal of the American College of Medical Genetics, 28(5), 102558. https://doi.org/10.1016/j.gim.2026.102558

Chicago Style (17th ed.) Citation

FC, Radio, et al. "Loss of Function of Retinol Dehydrogenase 11 Causes a Recessive Syndrome Characterized by Myopathy, Retinal Dystrophy, Juvenile Cataracts, and Microcephaly." Genetics in Medicine : Official Journal of the American College of Medical Genetics 28, no. 5 (2026): 102558. https://doi.org/10.1016/j.gim.2026.102558.

MLA (9th ed.) Citation

FC, Radio, et al. "Loss of Function of Retinol Dehydrogenase 11 Causes a Recessive Syndrome Characterized by Myopathy, Retinal Dystrophy, Juvenile Cataracts, and Microcephaly." Genetics in Medicine : Official Journal of the American College of Medical Genetics, vol. 28, no. 5, 2026, p. 102558, https://doi.org/10.1016/j.gim.2026.102558.