S. Bas Et Al. , "Thiamine Responsive Megaloblastic Anemia Due to SLCA19A2 Gene Mutation: Another Cause of Neonatal Diabetes with Succcesfull Switch from Insulin to Thiamine," HORMONE RESEARCH IN PAEDIATRICS , vol.86, pp.244, 2016
Bas, S. Et Al. 2016. Thiamine Responsive Megaloblastic Anemia Due to SLCA19A2 Gene Mutation: Another Cause of Neonatal Diabetes with Succcesfull Switch from Insulin to Thiamine. HORMONE RESEARCH IN PAEDIATRICS , vol.86 , 244.
Bas, S., Akbarzade, A., Atay, Z., Gurbanov, Z., GÜRAN, T., Turan, S., ... De Franco, E.(2016). Thiamine Responsive Megaloblastic Anemia Due to SLCA19A2 Gene Mutation: Another Cause of Neonatal Diabetes with Succcesfull Switch from Insulin to Thiamine. HORMONE RESEARCH IN PAEDIATRICS , vol.86, 244.
Bas, Serpil Et Al. "Thiamine Responsive Megaloblastic Anemia Due to SLCA19A2 Gene Mutation: Another Cause of Neonatal Diabetes with Succcesfull Switch from Insulin to Thiamine," HORMONE RESEARCH IN PAEDIATRICS , vol.86, 244, 2016
Bas, Serpil Et Al. "Thiamine Responsive Megaloblastic Anemia Due to SLCA19A2 Gene Mutation: Another Cause of Neonatal Diabetes with Succcesfull Switch from Insulin to Thiamine." HORMONE RESEARCH IN PAEDIATRICS , vol.86, pp.244, 2016
Bas, S. Et Al. (2016) . "Thiamine Responsive Megaloblastic Anemia Due to SLCA19A2 Gene Mutation: Another Cause of Neonatal Diabetes with Succcesfull Switch from Insulin to Thiamine." HORMONE RESEARCH IN PAEDIATRICS , vol.86, p.244.
@article{article, author={Serpil Bas Et Al. }, title={Thiamine Responsive Megaloblastic Anemia Due to SLCA19A2 Gene Mutation: Another Cause of Neonatal Diabetes with Succcesfull Switch from Insulin to Thiamine}, journal={HORMONE RESEARCH IN PAEDIATRICS}, year=2016, pages={244} }