Onat, O. E. Et Al. 2013. Missense mutation in the ATPase, aminophospholipid transporter protein ATP8A2 is associated with cerebellar atrophy and quadrupedal locomotion. EUROPEAN JOURNAL OF HUMAN GENETICS , vol.21, no.3 , 281-285.

Onat, O. E., Gulsuner, S., Bilguvar, K., Basak, A. N., Topaloglu, H., Tan, M., ... Tan, U.(2013). Missense mutation in the ATPase, aminophospholipid transporter protein ATP8A2 is associated with cerebellar atrophy and quadrupedal locomotion. EUROPEAN JOURNAL OF HUMAN GENETICS , vol.21, no.3, 281-285.

Onat, ONUR Et Al. "Missense mutation in the ATPase, aminophospholipid transporter protein ATP8A2 is associated with cerebellar atrophy and quadrupedal locomotion," EUROPEAN JOURNAL OF HUMAN GENETICS , vol.21, no.3, 281-285, 2013

Onat, ONUR E. Et Al. "Missense mutation in the ATPase, aminophospholipid transporter protein ATP8A2 is associated with cerebellar atrophy and quadrupedal locomotion." EUROPEAN JOURNAL OF HUMAN GENETICS , vol.21, no.3, pp.281-285, 2013

Onat, O. E. Et Al. (2013) . "Missense mutation in the ATPase, aminophospholipid transporter protein ATP8A2 is associated with cerebellar atrophy and quadrupedal locomotion." EUROPEAN JOURNAL OF HUMAN GENETICS , vol.21, no.3, pp.281-285.

@article{article, author={ONUR EMRE ONAT Et Al. }, title={Missense mutation in the ATPase, aminophospholipid transporter protein ATP8A2 is associated with cerebellar atrophy and quadrupedal locomotion}, journal={EUROPEAN JOURNAL OF HUMAN GENETICS}, year=2013, pages={281-285} }