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. , ...Daha Fazla

SSIEM 2016: Annual Symposium of the Society for the Study of Inborn Errors of Metabolism, Rome, Italy, 6 - 09 Eylül 2016

  • Yayın Türü: Bildiri / Özet Bildiri