E. Kose 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 , 1289-1293.
Kose, E., Armagan, C., Kisa, 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, Engin 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, Engin 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={Engin Kose Et Al. }, title={Severe hyperchylomicronemia in two infants with novel APOC2 gene mutation}, journal={JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM}, year=2018, pages={1289-1293} }