Per, H. 2013. A new variant detected in GRIN2A by whole-exome sequencing in a patient with intellectual disability with intractable epilepsy. EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY , vol.2013, no.17 , 63-64.

Per, H., (2013). A new variant detected in GRIN2A by whole-exome sequencing in a patient with intellectual disability with intractable epilepsy. EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY , vol.2013, no.17, 63-64.

Per, HÜSEYİN. "A new variant detected in GRIN2A by whole-exome sequencing in a patient with intellectual disability with intractable epilepsy," EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY , vol.2013, no.17, 63-64, 2013

Per, HÜSEYİN. "A new variant detected in GRIN2A by whole-exome sequencing in a patient with intellectual disability with intractable epilepsy." EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY , vol.2013, no.17, pp.63-64, 2013

Per, H. (2013) . "A new variant detected in GRIN2A by whole-exome sequencing in a patient with intellectual disability with intractable epilepsy." EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY , vol.2013, no.17, pp.63-64.

@article{article, author={HÜSEYİN PER}, title={A new variant detected in GRIN2A by whole-exome sequencing in a patient with intellectual disability with intractable epilepsy}, journal={EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY}, year=2013, pages={63-64} }