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., ...More

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

  • Publication Type: Conference Paper