A case with mitochondrial seryl t RNA synthetase gene SARS2 defect a novel mutation and a different phenotype from HUPRA syndrome

HİŞMİ B., BELOSTOTSKY R., ÜTİNE G. E., TALİM B., ÜNAL Ö., DURSUN A., ...Daha Fazla

12th International Congress of Inborn Errors of Metabolism, 3 - 06 Eylül 2013

  • Yayın Türü: Bildiri
  • Kocaeli Üniversitesi Adresli: Evet