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

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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