Molybdenum cofactor MOCO deficiency type B clinical biochemical and neuroimaging features of five patients with two novel mutations


HİŞMİ B., ÜNAL Ö., SASS J. O., BEERMAN F., ICHIDA K., DURSUN A., ...Daha Fazla

Annual Symposium of the Society for the Study of Inborn Errors of Metabolism, 4 - 07 Eylül 2012

  • Yayın Türü: Bildiri
  • Kocaeli Üniversitesi Adresli: Evet