ÖNENLİ MUNGAN, H. N. Et Al. 2016. 5 oxoprolinase deficiency report of three siblings and a case with two new compound heterozygous mutations and the clinical diversity even in the same family. SSIEM 2016 ROME .

ÖNENLİ MUNGAN, H. N., ŞEKER YILMAZ, B., BULUT, F. D., öktem, m., KÖR, D., ceylaner, g., ... HERGÜNER, M. Ö.(2016). 5 oxoprolinase deficiency report of three siblings and a case with two new compound heterozygous mutations and the clinical diversity even in the same family . SSIEM 2016 ROME

ÖNENLİ MUNGAN, HALİSE Et Al. "5 oxoprolinase deficiency report of three siblings and a case with two new compound heterozygous mutations and the clinical diversity even in the same family," SSIEM 2016 ROME, 2016

ÖNENLİ MUNGAN, HALİSE N. Et Al. "5 oxoprolinase deficiency report of three siblings and a case with two new compound heterozygous mutations and the clinical diversity even in the same family." SSIEM 2016 ROME , 2016

ÖNENLİ MUNGAN, H. N. Et Al. (2016) . "5 oxoprolinase deficiency report of three siblings and a case with two new compound heterozygous mutations and the clinical diversity even in the same family." SSIEM 2016 ROME .

@conferencepaper{conferencepaper, author={HALİSE NESLİHAN ÖNENLİ MUNGAN Et Al. }, title={5 oxoprolinase deficiency report of three siblings and a case with two new compound heterozygous mutations and the clinical diversity even in the same family}, congress name={SSIEM 2016 ROME}, city={}, country={}, year={2016}}