Celik, N. Et Al. 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 , vol.80, no.4 , 299-303.

Celik, N., CİNAZ, P., Emeksiz, H. C., Hussain, K., Camurdan, O., BİDECİ, A., ... DÖĞER, E.(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 , vol.80, no.4, 299-303.

Celik, 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, 299-303, 2013

Celik, 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, pp.299-303, 2013

Celik, N. Et Al. (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 , vol.80, no.4, pp.299-303.

@article{article, author={Nurullah Celik Et Al. }, title={Octreotide-Induced Long QT Syndrome in a Child with Congenital Hyperinsulinemia and a Novel Missense Mutation (p.Met115Val) in the ABCC8 Gene}, journal={HORMONE RESEARCH IN PAEDIATRICS}, year=2013, pages={299-303} }