Ütine, G. E. Et Al. 2013. A Homozygous Deletion in GRID2 Causes a Human Phenotype With Cerebellar Ataxia and Atrophy. JOURNAL OF CHILD NEUROLOGY , vol.28, no.7 , 926-932.

Ütine, G. E., Haliloglu, G., Volkan Salancı, B., Çetinkaya, A., Şimşek Kiper, P. Ö., Alanay, Y., ... Aktas, D.(2013). A Homozygous Deletion in GRID2 Causes a Human Phenotype With Cerebellar Ataxia and Atrophy. JOURNAL OF CHILD NEUROLOGY , vol.28, no.7, 926-932.

Ütine, GÜLEN Et Al. "A Homozygous Deletion in GRID2 Causes a Human Phenotype With Cerebellar Ataxia and Atrophy," JOURNAL OF CHILD NEUROLOGY , vol.28, no.7, 926-932, 2013

Ütine, GÜLEN E. Et Al. "A Homozygous Deletion in GRID2 Causes a Human Phenotype With Cerebellar Ataxia and Atrophy." JOURNAL OF CHILD NEUROLOGY , vol.28, no.7, pp.926-932, 2013

Ütine, G. E. Et Al. (2013) . "A Homozygous Deletion in GRID2 Causes a Human Phenotype With Cerebellar Ataxia and Atrophy." JOURNAL OF CHILD NEUROLOGY , vol.28, no.7, pp.926-932.

@article{article, author={GÜLEN EDA ÜTİNE Et Al. }, title={A Homozygous Deletion in GRID2 Causes a Human Phenotype With Cerebellar Ataxia and Atrophy}, journal={JOURNAL OF CHILD NEUROLOGY}, year=2013, pages={926-932} }