APA (7th ed.) Citation

H, J., A, A., S, F., X, F., Z, L., X, H., . . . F, F. (2022). Identification and characterization of novel MPC1 gene variants causing mitochondrial pyruvate carrier deficiency. Journal of inherited metabolic disease, 45(2), 264. https://doi.org/10.1002/jimd.12462

Chicago Style (17th ed.) Citation

H, Jiang, et al. "Identification and Characterization of Novel MPC1 Gene Variants Causing Mitochondrial Pyruvate Carrier Deficiency." Journal of Inherited Metabolic Disease 45, no. 2 (2022): 264. https://doi.org/10.1002/jimd.12462.

MLA (9th ed.) Citation

H, Jiang, et al. "Identification and Characterization of Novel MPC1 Gene Variants Causing Mitochondrial Pyruvate Carrier Deficiency." Journal of Inherited Metabolic Disease, vol. 45, no. 2, 2022, p. 264, https://doi.org/10.1002/jimd.12462.