APA (7th ed.) Citation

L, M., H, B., A, M., R, P., A, S., E, L., . . . B, P. (2021). Delineating the neurological phenotype in children with defects in the ECHS1 or HIBCH gene. Journal of inherited metabolic disease, 44(2), 401. https://doi.org/10.1002/jimd.12288

Chicago Style (17th ed.) Citation

L, Marti-Sanchez, et al. "Delineating the Neurological Phenotype in Children with Defects in the ECHS1 or HIBCH Gene." Journal of Inherited Metabolic Disease 44, no. 2 (2021): 401. https://doi.org/10.1002/jimd.12288.

MLA (9th ed.) Citation

L, Marti-Sanchez, et al. "Delineating the Neurological Phenotype in Children with Defects in the ECHS1 or HIBCH Gene." Journal of Inherited Metabolic Disease, vol. 44, no. 2, 2021, p. 401, https://doi.org/10.1002/jimd.12288.