Urea cycle disorders in India: clinical course, biochemical and genetic investigations, and prenatal testing.

MLA

Bijarnia-Mahay, Sunita, et al. “Urea Cycle Disorders in India: Clinical Course, Biochemical and Genetic Investigations, and Prenatal Testing.” Orphanet Journal of Rare Diseases, vol. 13, no. 1, Oct. 2018, p. 174. EBSCOhost, https://doi.org/10.1186/s13023-018-0908-1.

APA

Bijarnia-Mahay, S., Häberle, J., Jalan, A. B., Puri, R. D., Kohli, S., Kudalkar, K., Rüfenacht, V., Gupta, D., Maurya, D., Verma, J., Shigematsu, Y., Yamaguchi, S., Saxena, R., & Verma, I. C. (2018). Urea cycle disorders in India: clinical course, biochemical and genetic investigations, and prenatal testing. Orphanet Journal of Rare Diseases, 13(1), 174. https://doi.org/10.1186/s13023-018-0908-1

Chicago

Bijarnia-Mahay, Sunita, Johannes Häberle, Anil B Jalan, Ratna Dua Puri, Sudha Kohli, Ketki Kudalkar, Véronique Rüfenacht, et al. 2018. “Urea Cycle Disorders in India: Clinical Course, Biochemical and Genetic Investigations, and Prenatal Testing.” Orphanet Journal of Rare Diseases 13 (1): 174. doi:10.1186/s13023-018-0908-1.