Cite
Sudden death in an infant with 3-hydroxy-3-methylglutaryl-CoA lyase deficiency.
MLA
Ribes, A., et al. “Sudden Death in an Infant with 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency.” Journal of Inherited Metabolic Disease, vol. 13, no. 5, 1990, pp. 752–53. EBSCOhost, https://doi.org/10.1007/BF01799579.
APA
Ribes, A., Briones, P., Vilaseca, M. A., Baraibar, R., & Gairi, J. M. (1990). Sudden death in an infant with 3-hydroxy-3-methylglutaryl-CoA lyase deficiency. Journal of Inherited Metabolic Disease, 13(5), 752–753. https://doi.org/10.1007/BF01799579
Chicago
Ribes, A, P Briones, M A Vilaseca, R Baraibar, and J M Gairi. 1990. “Sudden Death in an Infant with 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency.” Journal of Inherited Metabolic Disease 13 (5): 752–53. doi:10.1007/BF01799579.