Cita APA (7a ed.)
Ali, E. Z., Zakaria, Y., Mohd Radzi, M. A., Ngu, L. H., & Jusoh, S. A. (2018). Mutation Study of Malaysian Patients with Ornithine Transcarbamylase Deficiency: Clinical, Molecular, and Bioinformatics Analyses of Two Novel Missense Mutations of the OTC Gene. BioMed Research International, 2018, 1-16.
Cita Chicago Style (17a ed.)
Ali, Ernie Zuraida, Yuslina Zakaria, Mohd Amran Mohd Radzi, Lock Hock Ngu, y Siti Azma Jusoh. "Mutation Study of Malaysian Patients with Ornithine Transcarbamylase Deficiency: Clinical, Molecular, and Bioinformatics Analyses of Two Novel Missense Mutations of the OTC Gene." BioMed Research International 2018 (2018): 1-16.
Cita MLA (9a ed.)
Ali, Ernie Zuraida, et al. "Mutation Study of Malaysian Patients with Ornithine Transcarbamylase Deficiency: Clinical, Molecular, and Bioinformatics Analyses of Two Novel Missense Mutations of the OTC Gene." BioMed Research International, vol. 2018, 2018, pp. 1-16.
Precaución: Estas citas no son 100% exactas.