ÜTİNE, 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.

ÜTİNE, G. E. , Haliloglu, G., Salanci, B., Cetinkaya, A., Kiper, P. O. , 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.

ÜTİNE, 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

ÜTİNE, 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

ÜTİNE, 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} }