T. Zubarioglu Et Al. , "Ornithine Aminotransferase Deficiency in Differential Diagnosis of Neonatal Hyperammonemia: A Case with a Novel OAT Gene Mutation," INDIAN JOURNAL OF PEDIATRICS , vol.83, no.7, pp.754-755, 2016
Zubarioglu, T. Et Al. 2016. Ornithine Aminotransferase Deficiency in Differential Diagnosis of Neonatal Hyperammonemia: A Case with a Novel OAT Gene Mutation. INDIAN JOURNAL OF PEDIATRICS , vol.83, no.7 , 754-755.
Zubarioglu, T., Kiykim, E., Cansever, M. S., & Zeybek, C. A., (2016). Ornithine Aminotransferase Deficiency in Differential Diagnosis of Neonatal Hyperammonemia: A Case with a Novel OAT Gene Mutation. INDIAN JOURNAL OF PEDIATRICS , vol.83, no.7, 754-755.
Zubarioglu, Tanyel Et Al. "Ornithine Aminotransferase Deficiency in Differential Diagnosis of Neonatal Hyperammonemia: A Case with a Novel OAT Gene Mutation," INDIAN JOURNAL OF PEDIATRICS , vol.83, no.7, 754-755, 2016
Zubarioglu, Tanyel Et Al. "Ornithine Aminotransferase Deficiency in Differential Diagnosis of Neonatal Hyperammonemia: A Case with a Novel OAT Gene Mutation." INDIAN JOURNAL OF PEDIATRICS , vol.83, no.7, pp.754-755, 2016
Zubarioglu, T. Et Al. (2016) . "Ornithine Aminotransferase Deficiency in Differential Diagnosis of Neonatal Hyperammonemia: A Case with a Novel OAT Gene Mutation." INDIAN JOURNAL OF PEDIATRICS , vol.83, no.7, pp.754-755.
@article{article, author={Tanyel Zubarioglu Et Al. }, title={Ornithine Aminotransferase Deficiency in Differential Diagnosis of Neonatal Hyperammonemia: A Case with a Novel OAT Gene Mutation}, journal={INDIAN JOURNAL OF PEDIATRICS}, year=2016, pages={754-755} }