DUNDAR, H. Et Al. 2012. Identification of a Novel Twinkle Mutation in a Family With Infantile Onset Spinocerebellar Ataxia by Whole Exome Sequencing. PEDIATRIC NEUROLOGY , vol.46, no.3 , 172-177.

DUNDAR, H., ÖZGÜL, R. K., YALNIZOĞLU, D., Erdem, S., Oguz, K. K., Tuncel, D., ... TEMUÇİN, Ç. M.(2012). Identification of a Novel Twinkle Mutation in a Family With Infantile Onset Spinocerebellar Ataxia by Whole Exome Sequencing. PEDIATRIC NEUROLOGY , vol.46, no.3, 172-177.

DUNDAR, Hall Et Al. "Identification of a Novel Twinkle Mutation in a Family With Infantile Onset Spinocerebellar Ataxia by Whole Exome Sequencing," PEDIATRIC NEUROLOGY , vol.46, no.3, 172-177, 2012

DUNDAR, Hall Et Al. "Identification of a Novel Twinkle Mutation in a Family With Infantile Onset Spinocerebellar Ataxia by Whole Exome Sequencing." PEDIATRIC NEUROLOGY , vol.46, no.3, pp.172-177, 2012

DUNDAR, H. Et Al. (2012) . "Identification of a Novel Twinkle Mutation in a Family With Infantile Onset Spinocerebellar Ataxia by Whole Exome Sequencing." PEDIATRIC NEUROLOGY , vol.46, no.3, pp.172-177.

@article{article, author={Hall DUNDAR Et Al. }, title={Identification of a Novel Twinkle Mutation in a Family With Infantile Onset Spinocerebellar Ataxia by Whole Exome Sequencing}, journal={PEDIATRIC NEUROLOGY}, year=2012, pages={172-177} }