APA (7th ed.) Citation

Habarou, F., Haack, T., Nitschke, P., Kölker, S., Korenke, C., & Marquardt, I. (2017). Biallelic mutations in LIPT2 cause a mitochondrial lipoylation defect associated with severe neonatal encephalopathy. The American journal of human genetics, 101(2), . https://doi.org/10.1016/j.ajhg.2017.07.001

Chicago Style (17th ed.) Citation

Habarou, Florence, Tobias Haack, Patrick Nitschke, Stefan Kölker, Christoph Korenke, and Iris Marquardt. "Biallelic Mutations in LIPT2 Cause a Mitochondrial Lipoylation Defect Associated with Severe Neonatal Encephalopathy." The American Journal of Human Genetics 101, no. 2 (2017). https://doi.org/10.1016/j.ajhg.2017.07.001.

MLA (9th ed.) Citation

Habarou, Florence, et al. "Biallelic Mutations in LIPT2 Cause a Mitochondrial Lipoylation Defect Associated with Severe Neonatal Encephalopathy." The American Journal of Human Genetics, vol. 101, no. 2, 2017, https://doi.org/10.1016/j.ajhg.2017.07.001.