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