KAYA ÖZÇORA, G. D. Et Al. 2017. Coenzyme Q10 deficiency A treatable autosomal recessive cerebellar ataxias. EPNS 2017 - 12th European Paediatric Neurology Society CongressLyon, France20- 24 June 2017 , 136.

KAYA ÖZÇORA, G. D., BAŞAK, N., CANPOLAT, M., ACER, H., & KUMANDAŞ, S., (2017). Coenzyme Q10 deficiency A treatable autosomal recessive cerebellar ataxias . EPNS 2017 - 12th European Paediatric Neurology Society CongressLyon, France20- 24 June 2017 (pp.136).

KAYA ÖZÇORA, Gül Et Al. "Coenzyme Q10 deficiency A treatable autosomal recessive cerebellar ataxias," EPNS 2017 - 12th European Paediatric Neurology Society CongressLyon, France20- 24 June 2017, 2017

KAYA ÖZÇORA, Gül D. Et Al. "Coenzyme Q10 deficiency A treatable autosomal recessive cerebellar ataxias." EPNS 2017 - 12th European Paediatric Neurology Society CongressLyon, France20- 24 June 2017 , pp.136, 2017

KAYA ÖZÇORA, G. D. Et Al. (2017) . "Coenzyme Q10 deficiency A treatable autosomal recessive cerebellar ataxias." EPNS 2017 - 12th European Paediatric Neurology Society CongressLyon, France20- 24 June 2017 , p.136.

@conferencepaper{conferencepaper, author={Gül Demet KAYA ÖZÇORA Et Al. }, title={Coenzyme Q10 deficiency A treatable autosomal recessive cerebellar ataxias}, congress name={EPNS 2017 - 12th European Paediatric Neurology Society CongressLyon, France20- 24 June 2017}, city={}, country={}, year={2017}, pages={136} }