Olgac, A. Et Al. 2020. Carbonic anhydrase VA deficiency: a very rare case of hyperammonemic encephalopathy. JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.33 , 1349-1352.

Olgac, A., Kasapkara, C. S. , Kilic, M., Keskin, E. Y. , SANDAL, G., Cram, D. S. , ... Haberle, J.(2020). Carbonic anhydrase VA deficiency: a very rare case of hyperammonemic encephalopathy. JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.33, 1349-1352.

Olgac, Asburce Et Al. "Carbonic anhydrase VA deficiency: a very rare case of hyperammonemic encephalopathy," JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.33, 1349-1352, 2020

Olgac, Asburce Et Al. "Carbonic anhydrase VA deficiency: a very rare case of hyperammonemic encephalopathy." JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.33, pp.1349-1352, 2020

Olgac, A. Et Al. (2020) . "Carbonic anhydrase VA deficiency: a very rare case of hyperammonemic encephalopathy." JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.33, pp.1349-1352.

@article{article, author={Asburce Olgac Et Al. }, title={Carbonic anhydrase VA deficiency: a very rare case of hyperammonemic encephalopathy}, journal={JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM}, year=2020, pages={1349-1352} }