BAŞ, 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. 55th Annual Meeting of the ESPE , 244.

BAŞ, 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 . 55th Annual Meeting of the ESPE (pp.244).

BAŞ, SERPİL Et Al. "Thiamine Responsive Megaloblastic Anemia Due to SLCA19A2 Gene Mutation Another Cause of Neonatal Diabetes with Succcesfull Switch from Insulin to Thiamine," 55th Annual Meeting of the ESPE, 2016

BAŞ, SERPİL Et Al. "Thiamine Responsive Megaloblastic Anemia Due to SLCA19A2 Gene Mutation Another Cause of Neonatal Diabetes with Succcesfull Switch from Insulin to Thiamine." 55th Annual Meeting of the ESPE , pp.244, 2016

BAŞ, 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." 55th Annual Meeting of the ESPE , p.244.

@conferencepaper{conferencepaper, author={SERPİL BAŞ Et Al. }, title={Thiamine Responsive Megaloblastic Anemia Due to SLCA19A2 Gene Mutation Another Cause of Neonatal Diabetes with Succcesfull Switch from Insulin to Thiamine}, congress name={55th Annual Meeting of the ESPE}, city={}, country={}, year={2016}, pages={244} }