APA (7th ed.) Citation

J, S., W, G., D, P., BS, A., RK, O., M, O., . . . E, P. (2011). Urgent metabolic service improves survival in long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency detected by symptomatic identification and pilot newborn screening. Journal of inherited metabolic disease, 34(1), 185. https://doi.org/10.1007/s10545-010-9244-x

Chicago Style (17th ed.) Citation

J, Sykut-Cegielska, et al. "Urgent Metabolic Service Improves Survival in Long-chain 3-hydroxyacyl-CoA Dehydrogenase (LCHAD) Deficiency Detected by Symptomatic Identification and Pilot Newborn Screening." Journal of Inherited Metabolic Disease 34, no. 1 (2011): 185. https://doi.org/10.1007/s10545-010-9244-x.

MLA (9th ed.) Citation

J, Sykut-Cegielska, et al. "Urgent Metabolic Service Improves Survival in Long-chain 3-hydroxyacyl-CoA Dehydrogenase (LCHAD) Deficiency Detected by Symptomatic Identification and Pilot Newborn Screening." Journal of Inherited Metabolic Disease, vol. 34, no. 1, 2011, p. 185, https://doi.org/10.1007/s10545-010-9244-x.