Kasapkara, C. S. Et Al. 2019. An infant with an extremely rare cobalamin disorder: Methionine synthase deficiency and importance of early diagnosis and treatment. TURKISH JOURNAL OF PEDIATRICS , vol.61 , 282-285.

Kasapkara, C. S. , YILMAZ KESKİN, E., Ozbay-Hosnut, F., Akcaboy, M., Polat, E., Olgac, A., ... Zorlu, P.(2019). An infant with an extremely rare cobalamin disorder: Methionine synthase deficiency and importance of early diagnosis and treatment. TURKISH JOURNAL OF PEDIATRICS , vol.61, 282-285.

Kasapkara, Cigdem Et Al. "An infant with an extremely rare cobalamin disorder: Methionine synthase deficiency and importance of early diagnosis and treatment," TURKISH JOURNAL OF PEDIATRICS , vol.61, 282-285, 2019

Kasapkara, Cigdem S. Et Al. "An infant with an extremely rare cobalamin disorder: Methionine synthase deficiency and importance of early diagnosis and treatment." TURKISH JOURNAL OF PEDIATRICS , vol.61, pp.282-285, 2019

Kasapkara, C. S. Et Al. (2019) . "An infant with an extremely rare cobalamin disorder: Methionine synthase deficiency and importance of early diagnosis and treatment." TURKISH JOURNAL OF PEDIATRICS , vol.61, pp.282-285.

@article{article, author={Cigdem Seher Kasapkara Et Al. }, title={An infant with an extremely rare cobalamin disorder: Methionine synthase deficiency and importance of early diagnosis and treatment}, journal={TURKISH JOURNAL OF PEDIATRICS}, year=2019, pages={282-285} }