Clinical and laboratory features of phenylalanine hydroxylase deficient phenylketonuria patients developing secondary unresponsiveness to sapropterin treatment

COŞKUN T., ÜNAL Ö., GÖKMEN ÖZEL H., ÖZGÜL R. K., YÜCEL YILMAZ D., DURSUN A., ...Daha Fazla

Annual Symposium of the Society for the Study of Inborn Errors of Metabolism, 2 - 05 Eylül 2014

• Yayın Türü: Bildiri
• Kocaeli Üniversitesi Adresli: Evet