Identification of a novel mutation in Turkish infant with early onset monocarboxylate transporter 1 MCT1 deficiency as a cause of recurrent ketoacidosis

OKUR İ., İNCİ A., KELEŞ E., KARAOĞLU A., Ceylaner S., BİBEROĞLU G., ...More

SSIEM 2016: Annual Symposium of the Society for the Study of Inborn Errors of Metabolism, Rome, Italy, 6 - 09 September 2016, (Summary Text)

• Publication Type: Conference Paper / Summary Text
• Gazi University Affiliated: Yes