Kara, E. Et Al. 2021. Glycogen storage disease type XII; An ultra rare cause of hemolytic anemia and rhabdomyolysis: One new case report. Journal of Pediatric Endocrinology and Metabolism , vol.34, no.10 , 1335-1339.

Kara, E., KOR, D., Bulut, F. D., Hergüner, Ö., CEYLANER, S., Köşeci, B., ... BURGAÇ, E.(2021). Glycogen storage disease type XII; An ultra rare cause of hemolytic anemia and rhabdomyolysis: One new case report. Journal of Pediatric Endocrinology and Metabolism , vol.34, no.10, 1335-1339.

Kara, Esra Et Al. "Glycogen storage disease type XII; An ultra rare cause of hemolytic anemia and rhabdomyolysis: One new case report," Journal of Pediatric Endocrinology and Metabolism , vol.34, no.10, 1335-1339, 2021

Kara, Esra Et Al. "Glycogen storage disease type XII; An ultra rare cause of hemolytic anemia and rhabdomyolysis: One new case report." Journal of Pediatric Endocrinology and Metabolism , vol.34, no.10, pp.1335-1339, 2021

Kara, E. Et Al. (2021) . "Glycogen storage disease type XII; An ultra rare cause of hemolytic anemia and rhabdomyolysis: One new case report." Journal of Pediatric Endocrinology and Metabolism , vol.34, no.10, pp.1335-1339.

@article{article, author={Esra Kara Et Al. }, title={Glycogen storage disease type XII; An ultra rare cause of hemolytic anemia and rhabdomyolysis: One new case report}, journal={Journal of Pediatric Endocrinology and Metabolism}, year=2021, pages={1335-1339} }