Cite
Octreotide-Induced Long QT Syndrome in a Child with Congenital Hyperinsulinemia and a Novel Missense Mutation (p.Met115Val) in the ABCC8 Gene.
MLA
Çelik, Nurullah, et al. “Octreotide-Induced Long QT Syndrome in a Child with Congenital Hyperinsulinemia and a Novel Missense Mutation (p.Met115Val) in the ABCC8 Gene.” Hormone Research in Paediatrics, vol. 80, no. 4, Oct. 2013, pp. 299–303. EBSCOhost, https://doi.org/10.1159/000354666.
APA
Çelik, N., Cinaz, P., Emeksiz, H. C., Hussain, K., Çamurdan, O., Bideci, aysun, Döğer, E., Yüce, Ö., Türkyılmaz, Z., & Oğuz, ayşe D. (2013). Octreotide-Induced Long QT Syndrome in a Child with Congenital Hyperinsulinemia and a Novel Missense Mutation (p.Met115Val) in the ABCC8 Gene. Hormone Research in Paediatrics, 80(4), 299–303. https://doi.org/10.1159/000354666
Chicago
Çelik, Nurullah, Peyami Cinaz, Hamdi Cihan Emeksiz, Khalid Hussain, Orhun Çamurdan, aysun Bideci, Esra Döğer, Özge Yüce, Zafer Türkyılmaz, and ayşe Deniz Oğuz. 2013. “Octreotide-Induced Long QT Syndrome in a Child with Congenital Hyperinsulinemia and a Novel Missense Mutation (p.Met115Val) in the ABCC8 Gene.” Hormone Research in Paediatrics 80 (4): 299–303. doi:10.1159/000354666.