Kose, E. Et Al. 2018. Severe hyperchylomicronemia in two infants with novel APOC2 gene mutation. JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.31, no.11 , 1289-1293.

Kose, E., ARMAĞAN, C., Teke Klsa, P., Onay, H., & Arslan, N., (2018). Severe hyperchylomicronemia in two infants with novel APOC2 gene mutation. JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.31, no.11, 1289-1293.

Kose, ENGİN Et Al. "Severe hyperchylomicronemia in two infants with novel APOC2 gene mutation," JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.31, no.11, 1289-1293, 2018

Kose, ENGİN Et Al. "Severe hyperchylomicronemia in two infants with novel APOC2 gene mutation." JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.31, no.11, pp.1289-1293, 2018

Kose, E. Et Al. (2018) . "Severe hyperchylomicronemia in two infants with novel APOC2 gene mutation." JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.31, no.11, pp.1289-1293.

@article{article, author={ENGİN KÖSE Et Al. }, title={Severe hyperchylomicronemia in two infants with novel APOC2 gene mutation}, journal={JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM}, year=2018, pages={1289-1293} }