APA (7th ed.) Citation

H, L., Q, M., Y, X., L, C., L, B., L, H., . . . F, Z. (2025). Compound heterozygous mutation of AFG3L2 causes autosomal recessive spinocerebellar ataxia through mitochondrial impairment and MICU1 mediated Ca2+ overload. Science China. Life sciences, 68(2), 484. https://doi.org/10.1007/s11427-023-2549-2

Chicago Style (17th ed.) Citation

H, Li, et al. "Compound Heterozygous Mutation of AFG3L2 Causes Autosomal Recessive Spinocerebellar Ataxia Through Mitochondrial Impairment and MICU1 Mediated Ca2+ Overload." Science China. Life Sciences 68, no. 2 (2025): 484. https://doi.org/10.1007/s11427-023-2549-2.

MLA (9th ed.) Citation

H, Li, et al. "Compound Heterozygous Mutation of AFG3L2 Causes Autosomal Recessive Spinocerebellar Ataxia Through Mitochondrial Impairment and MICU1 Mediated Ca2+ Overload." Science China. Life Sciences, vol. 68, no. 2, 2025, p. 484, https://doi.org/10.1007/s11427-023-2549-2.