Cite
A new type of defect in the gene for bilirubin uridine 5'-diphosphate-glucuronosyltransferase in a patient with Crigler-Najjar syndrome type I.
MLA
Aono, S., et al. “A New Type of Defect in the Gene for Bilirubin Uridine 5’-Diphosphate-Glucuronosyltransferase in a Patient with Crigler-Najjar Syndrome Type I.” Pediatric Research, vol. 35, no. 6, June 1994, pp. 629–32. EBSCOhost, https://doi.org/10.1203/00006450-199406000-00002.
APA
Aono, S., Yamada, Y., Keino, H., Sasaoka, Y., Nakagawa, T., Onishi, S., Mimura, S., Koiwai, O., & Sato, H. (1994). A new type of defect in the gene for bilirubin uridine 5’-diphosphate-glucuronosyltransferase in a patient with Crigler-Najjar syndrome type I. Pediatric Research, 35(6), 629–632. https://doi.org/10.1203/00006450-199406000-00002
Chicago
Aono, S, Y Yamada, H Keino, Y Sasaoka, T Nakagawa, S Onishi, S Mimura, O Koiwai, and H Sato. 1994. “A New Type of Defect in the Gene for Bilirubin Uridine 5’-Diphosphate-Glucuronosyltransferase in a Patient with Crigler-Najjar Syndrome Type I.” Pediatric Research 35 (6): 629–32. doi:10.1203/00006450-199406000-00002.