Abrams, A. J., Hufnagel, R. B., Rebelo, A., Zanna, C., Patel, N., Gonzalez, M. A., et al. (2015). Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder. Nature Genetics, 47(8), 926-32. https://doi.org/10.1038/ng.3354
Xie, Y., Wu, X., Tao, S., Wan, Y., & Tao, F. (2022). Development and validation of the self-rating of biological rhythm disorder for Chinese adolescents. Chronobiology International, 39(2), 198-204. https://doi.org/10.1080/07420528.2021.1989450
