Cakmak Celik, F. Et Al. 2021. A newborn case of adenylosuccinate lyase deficiency with a novel heterozygous mutation diagnosed by whole exome sequencing. Clinical Neurology and Neurosurgery , vol.202 .

Cakmak Celik, F., Ozlu, M. M., & CEYLANER, S., (2021). A newborn case of adenylosuccinate lyase deficiency with a novel heterozygous mutation diagnosed by whole exome sequencing. Clinical Neurology and Neurosurgery , vol.202.

Cakmak Celik, Fatma, Mehmet Mustafa Ozlu, And SERDAR CEYLANER. "A newborn case of adenylosuccinate lyase deficiency with a novel heterozygous mutation diagnosed by whole exome sequencing," Clinical Neurology and Neurosurgery , vol.202, 2021

Cakmak Celik, Fatma C. Et Al. "A newborn case of adenylosuccinate lyase deficiency with a novel heterozygous mutation diagnosed by whole exome sequencing." Clinical Neurology and Neurosurgery , vol.202, 2021

Cakmak Celik, F. Ozlu, M. M. And CEYLANER, S. (2021) . "A newborn case of adenylosuccinate lyase deficiency with a novel heterozygous mutation diagnosed by whole exome sequencing." Clinical Neurology and Neurosurgery , vol.202.

@article{article, author={Fatma Cakmak Celik Et Al. }, title={A newborn case of adenylosuccinate lyase deficiency with a novel heterozygous mutation diagnosed by whole exome sequencing}, journal={Clinical Neurology and Neurosurgery}, year=2021}