Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome: a treatable genetic liver disease warranting urgent diagnosis.

MLA

Lee, Hencher H. C., et al. “Hyperornithinaemia-Hyperammonaemia-Homocitrullinuria Syndrome: A Treatable Genetic Liver Disease Warranting Urgent Diagnosis.” Hong Kong Medical Journal = Xianggang Yi Xue Za Zhi, vol. 20, no. 1, Feb. 2014, pp. 63–66. EBSCOhost, https://doi.org/10.12809/hkmj133826.

APA

Lee, H. H. C., Poon, K. H., Lai, C. K., Au, K. M., Siu, T. S., Lai, J. P. S., Mak, C. M., Yuen, Y. P., Lam, C. W., & Chan, A. Y. W. (2014). Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome: a treatable genetic liver disease warranting urgent diagnosis. Hong Kong Medical Journal = Xianggang Yi Xue Za Zhi, 20(1), 63–66. https://doi.org/10.12809/hkmj133826

Chicago

Lee, Hencher H C, K H Poon, C K Lai, K M Au, T S Siu, Judy P S Lai, Chloe M Mak, Y P Yuen, C W Lam, and Albert Y W Chan. 2014. “Hyperornithinaemia-Hyperammonaemia-Homocitrullinuria Syndrome: A Treatable Genetic Liver Disease Warranting Urgent Diagnosis.” Hong Kong Medical Journal = Xianggang Yi Xue Za Zhi 20 (1): 63–66. doi:10.12809/hkmj133826.