Double trouble in an encephalopathic newborn citrullinemia and profound biotinidase deficiency


MÜMİNOĞLUTAHTA N., HİŞMİ B., ÜNAL Ö. , SİVRİ H. S. , DURSUN A., TOKATLI A., ...More

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

  • Publication Type: Conference Paper