Kilic, M. Et Al. 2019. Exon 2 deletion represents a common mutation in Turkish patients with fructose-1,6-bisphosphatase deficiency. METABOLIC BRAIN DISEASE , vol.34, no.5 , 1487-1491.

Kilic, M., Kasapkara, C. S., Yilmaz, D. Y., & Ozguel, R. K., (2019). Exon 2 deletion represents a common mutation in Turkish patients with fructose-1,6-bisphosphatase deficiency. METABOLIC BRAIN DISEASE , vol.34, no.5, 1487-1491.

Kilic, Mustafa Et Al. "Exon 2 deletion represents a common mutation in Turkish patients with fructose-1,6-bisphosphatase deficiency," METABOLIC BRAIN DISEASE , vol.34, no.5, 1487-1491, 2019

Kilic, Mustafa Et Al. "Exon 2 deletion represents a common mutation in Turkish patients with fructose-1,6-bisphosphatase deficiency." METABOLIC BRAIN DISEASE , vol.34, no.5, pp.1487-1491, 2019

Kilic, M. Et Al. (2019) . "Exon 2 deletion represents a common mutation in Turkish patients with fructose-1,6-bisphosphatase deficiency." METABOLIC BRAIN DISEASE , vol.34, no.5, pp.1487-1491.

@article{article, author={Mustafa Kilic Et Al. }, title={Exon 2 deletion represents a common mutation in Turkish patients with fructose-1,6-bisphosphatase deficiency}, journal={METABOLIC BRAIN DISEASE}, year=2019, pages={1487-1491} }