APA (7th ed.) Citation

Al-Thihli, K., Afting, C., Al-Hashmi, N., Mohammed, M., Sliwinski, S. C., Al Shibli, N., . . . Al-Maawali, A. (2021). Deficiency of acyl-CoA synthetase 5 is associated with a severe and treatable failure to thrive of neonatal onset. Clinical genetics, 99(3), . https://doi.org/10.1111/cge.13883

Chicago Style (17th ed.) Citation

Al-Thihli, Khalid, et al. "Deficiency of Acyl-CoA Synthetase 5 Is Associated with a Severe and Treatable Failure to Thrive of Neonatal Onset." Clinical Genetics 99, no. 3 (2021). https://doi.org/10.1111/cge.13883.

MLA (9th ed.) Citation

Al-Thihli, Khalid, et al. "Deficiency of Acyl-CoA Synthetase 5 Is Associated with a Severe and Treatable Failure to Thrive of Neonatal Onset." Clinical Genetics, vol. 99, no. 3, 2021, https://doi.org/10.1111/cge.13883.