APA (7th ed.) Citation

Pitt, J. J., Peters, H., Boneh, A., Yaplito‐Lee, J., Wieser, S., Hinderhofer, K., . . . Zschocke, J. (2015). Mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency: Urinary organic acid profiles and expanded spectrum of mutations. Journal of inherited metabolic disease, 38(3), . https://doi.org/10.1007/s10545-014-9801-9

Chicago Style (17th ed.) Citation

Pitt, James J., Heidi Peters, Avihu Boneh, Joy Yaplito‐Lee, Stefanie Wieser, Katrin Hinderhofer, David Johnson, and Johannes Zschocke. "Mitochondrial 3-hydroxy-3-methylglutaryl-CoA Synthase Deficiency: Urinary Organic Acid Profiles and Expanded Spectrum of Mutations." Journal of Inherited Metabolic Disease 38, no. 3 (2015). https://doi.org/10.1007/s10545-014-9801-9.

MLA (9th ed.) Citation

Pitt, James J., et al. "Mitochondrial 3-hydroxy-3-methylglutaryl-CoA Synthase Deficiency: Urinary Organic Acid Profiles and Expanded Spectrum of Mutations." Journal of Inherited Metabolic Disease, vol. 38, no. 3, 2015, https://doi.org/10.1007/s10545-014-9801-9.