APA (7th ed.) Citation

Shahrour, M., Staretz‐Chacham, O., Dayan, D., Stephen, J., Weech, A., Damseh, N., . . . Malicdan, M. (2017). Mitochondrial epileptic encephalopathy, 3-methylglutaconic aciduria and variable complex V deficiency associated with TIMM50 mutations. Clinical Genetics, 91(5), 690. https://doi.org/10.1111/cge.12855

Chicago Style (17th ed.) Citation

Shahrour, M.A, et al. "Mitochondrial Epileptic Encephalopathy, 3-methylglutaconic Aciduria and Variable Complex V Deficiency Associated with TIMM50 Mutations." Clinical Genetics 91, no. 5 (2017): 690. https://doi.org/10.1111/cge.12855.

MLA (9th ed.) Citation

Shahrour, M.A, et al. "Mitochondrial Epileptic Encephalopathy, 3-methylglutaconic Aciduria and Variable Complex V Deficiency Associated with TIMM50 Mutations." Clinical Genetics, vol. 91, no. 5, 2017, p. 690, https://doi.org/10.1111/cge.12855.