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

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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