ÖNENLİ MUNGAN, H. N. Et Al. 2016. Oxoprolinase deficiency report of three siblings ans a case with two new compound heterozygous mutations and the clinical diversity even in the same family. Annual Symposium of the Society for the Study of Inborn Errors of Metabolism .

ÖNENLİ MUNGAN, H. N., ŞEKER YILMAZ, B., BULUT, F. D., OKTEM, M., KÖR, D., CEYLANER, S., ... HERGÜNER, M. Ö.(2016). Oxoprolinase deficiency report of three siblings ans a case with two new compound heterozygous mutations and the clinical diversity even in the same family . Annual Symposium of the Society for the Study of Inborn Errors of Metabolism

ÖNENLİ MUNGAN, HALİSE Et Al. "Oxoprolinase deficiency report of three siblings ans a case with two new compound heterozygous mutations and the clinical diversity even in the same family," Annual Symposium of the Society for the Study of Inborn Errors of Metabolism, 2016

ÖNENLİ MUNGAN, HALİSE N. Et Al. "Oxoprolinase deficiency report of three siblings ans a case with two new compound heterozygous mutations and the clinical diversity even in the same family." Annual Symposium of the Society for the Study of Inborn Errors of Metabolism , 2016

ÖNENLİ MUNGAN, H. N. Et Al. (2016) . "Oxoprolinase deficiency report of three siblings ans a case with two new compound heterozygous mutations and the clinical diversity even in the same family." Annual Symposium of the Society for the Study of Inborn Errors of Metabolism .

@conferencepaper{conferencepaper, author={HALİSE NESLİHAN ÖNENLİ MUNGAN Et Al. }, title={Oxoprolinase deficiency report of three siblings ans a case with two new compound heterozygous mutations and the clinical diversity even in the same family}, congress name={Annual Symposium of the Society for the Study of Inborn Errors of Metabolism}, city={}, country={}, year={2016}}