A patient with a novel mutation in the GALT gene and initially misdiagnosed with a Congenital Glycolysation Defect

GÜNDÜZ M., ÖZAYDIN E., KOÇ N., KIRSAÇLIOĞLU C., ÜNAL S., ÜNAL Ö.

Annual Symposium of the Society for the Study of Inborn Errors of Metabolism, 1 - 04 Eylül 2015

  • Yayın Türü: Bildiri
  • Kocaeli Üniversitesi Adresli: Evet