H. ACER Et Al. , "A familial case of Leigh Disease related to NDUFV1 homozygous mutations," EPNS 2017 - 12th European Paediatric Neurology Society CongressLyon, France 20- 24 June 2017 , vol.21, pp.133-134, 2017
ACER, H. Et Al. 2017. A familial case of Leigh Disease related to NDUFV1 homozygous mutations. EPNS 2017 - 12th European Paediatric Neurology Society CongressLyon, France 20- 24 June 2017 , 133-134.
ACER, H., CANPOLAT, M., KAYA ÖZÇORA, G. D., & KUMANDAŞ, S., (2017). A familial case of Leigh Disease related to NDUFV1 homozygous mutations . EPNS 2017 - 12th European Paediatric Neurology Society CongressLyon, France 20- 24 June 2017 (pp.133-134).
ACER, HAMİT Et Al. "A familial case of Leigh Disease related to NDUFV1 homozygous mutations," EPNS 2017 - 12th European Paediatric Neurology Society CongressLyon, France 20- 24 June 2017, 2017
ACER, HAMİT Et Al. "A familial case of Leigh Disease related to NDUFV1 homozygous mutations." EPNS 2017 - 12th European Paediatric Neurology Society CongressLyon, France 20- 24 June 2017 , pp.133-134, 2017
ACER, H. Et Al. (2017) . "A familial case of Leigh Disease related to NDUFV1 homozygous mutations." EPNS 2017 - 12th European Paediatric Neurology Society CongressLyon, France 20- 24 June 2017 , pp.133-134.
@conferencepaper{conferencepaper, author={HAMİT ACER Et Al. }, title={A familial case of Leigh Disease related to NDUFV1 homozygous mutations}, congress name={EPNS 2017 - 12th European Paediatric Neurology Society CongressLyon, France 20- 24 June 2017}, city={}, country={}, year={2017}, pages={133-134} }