Hepatic phenotypes of HNF1B gene mutations: a case of neonatal cholestasis requiring portoenterostomy and literature review.

MLA

Kotalova, Radana, et al. “Hepatic Phenotypes of HNF1B Gene Mutations: A Case of Neonatal Cholestasis Requiring Portoenterostomy and Literature Review.” World Journal of Gastroenterology, vol. 21, no. 8, Feb. 2015, pp. 2550–57. EBSCOhost, https://doi.org/10.3748/wjg.v21.i8.2550.

APA

Kotalova, R., Dusatkova, P., Cinek, O., Dusatkova, L., Dedic, T., Seeman, T., Lebl, J., & Pruhova, S. (2015). Hepatic phenotypes of HNF1B gene mutations: a case of neonatal cholestasis requiring portoenterostomy and literature review. World Journal of Gastroenterology, 21(8), 2550–2557. https://doi.org/10.3748/wjg.v21.i8.2550

Chicago

Kotalova, Radana, Petra Dusatkova, Ondrej Cinek, Lenka Dusatkova, Tomas Dedic, Tomas Seeman, Jan Lebl, and Stepanka Pruhova. 2015. “Hepatic Phenotypes of HNF1B Gene Mutations: A Case of Neonatal Cholestasis Requiring Portoenterostomy and Literature Review.” World Journal of Gastroenterology 21 (8): 2550–57. doi:10.3748/wjg.v21.i8.2550.