COŞKUN, T. Et Al. 2014. Clinical and laboratory features of phenylalanine hydroxylase deficient phenylketonuria patients developing secondary unresponsiveness to sapropterin treatment. Annual Symposium of the Society for the Study of Inborn Errors of Metabolism .

COŞKUN, T., ÜNAL, Ö., GÖKMEN ÖZEL, H., ÖZGÜL, R. K., YÜCEL YILMAZ, D., DURSUN, A., ... TOKATLI, A.(2014). Clinical and laboratory features of phenylalanine hydroxylase deficient phenylketonuria patients developing secondary unresponsiveness to sapropterin treatment . Annual Symposium of the Society for the Study of Inborn Errors of Metabolism

COŞKUN, TURGAY Et Al. "Clinical and laboratory features of phenylalanine hydroxylase deficient phenylketonuria patients developing secondary unresponsiveness to sapropterin treatment," Annual Symposium of the Society for the Study of Inborn Errors of Metabolism, 2014

COŞKUN, TURGAY Et Al. "Clinical and laboratory features of phenylalanine hydroxylase deficient phenylketonuria patients developing secondary unresponsiveness to sapropterin treatment." Annual Symposium of the Society for the Study of Inborn Errors of Metabolism , 2014

COŞKUN, T. Et Al. (2014) . "Clinical and laboratory features of phenylalanine hydroxylase deficient phenylketonuria patients developing secondary unresponsiveness to sapropterin treatment." Annual Symposium of the Society for the Study of Inborn Errors of Metabolism .

@conferencepaper{conferencepaper, author={TURGAY COŞKUN Et Al. }, title={Clinical and laboratory features of phenylalanine hydroxylase deficient phenylketonuria patients developing secondary unresponsiveness to sapropterin treatment}, congress name={Annual Symposium of the Society for the Study of Inborn Errors of Metabolism}, city={}, country={}, year={2014}}