Identification of a novel deletion in UDP-glucuronosyltransferase gene in a patient with Crigler-Najjar syndrome type I.

MLA

Costa, Elísio, et al. “Identification of a Novel Deletion in UDP-Glucuronosyltransferase Gene in a Patient with Crigler-Najjar Syndrome Type I.” Blood Cells, Molecules & Diseases, vol. 42, no. 3, May 2009, pp. 265–66. EBSCOhost, https://doi.org/10.1016/j.bcmd.2008.12.004.

APA

Costa, E., Vieira, E., Lopes, A. I., Saldanha, M. J., Brites, D., & Dos Santos, R. (2009). Identification of a novel deletion in UDP-glucuronosyltransferase gene in a patient with Crigler-Najjar syndrome type I. Blood Cells, Molecules & Diseases, 42(3), 265–266. https://doi.org/10.1016/j.bcmd.2008.12.004

Chicago

Costa, Elísio, Emília Vieira, Ana Isabel Lopes, Maria Joana Saldanha, Dora Brites, and Rosário Dos Santos. 2009. “Identification of a Novel Deletion in UDP-Glucuronosyltransferase Gene in a Patient with Crigler-Najjar Syndrome Type I.” Blood Cells, Molecules & Diseases 42 (3): 265–66. doi:10.1016/j.bcmd.2008.12.004.