α-Methyl-CoA Racemase Deficiency: Report of A New Mutation and Response To Treatment in A Patient with Neonatal Cholestatic Liver Disease and Attention Deficit Hyperactivity Disorder

ERSOY M., ÇAKIR BİÇER N., BALCI M. C., DEMİRKOL M., GÖKÇAY G. F.

2012 Annual Symposium of the Society for the Study of Inborn Errors of Metabolism-United Kingdom, 4 - 07 Eylül 2012, (Özet Bildiri)

• Yayın Türü: Bildiri / Özet Bildiri
• İstanbul Üniversitesi Adresli: Evet