DÜNDAR, H. Et Al. 2011. Next generation sequencing in a family with infantile onset spinocerebellar ataxia identified a novel missense mutation in C10orf2 gene. European Human Genetics Conference , (Amsterdam, Netherlands), 11.

DÜNDAR, H., ÖZGÜL, R. K., YALNIZOĞLU, D., ERDEM ÖZDAMAR, S., TUNCEL, D., AKARSU, A. N., ... DURSUN, A.(2011). Next generation sequencing in a family with infantile onset spinocerebellar ataxia identified a novel missense mutation in C10orf2 gene . European Human Genetics Conference (pp.11). Amsterdam, Netherlands

DÜNDAR, HALİL Et Al. "Next generation sequencing in a family with infantile onset spinocerebellar ataxia identified a novel missense mutation in C10orf2 gene," European Human Genetics Conference, Amsterdam, Netherlands, 2011

DÜNDAR, HALİL Et Al. "Next generation sequencing in a family with infantile onset spinocerebellar ataxia identified a novel missense mutation in C10orf2 gene." European Human Genetics Conference , Amsterdam, Netherlands, pp.11, 2011

DÜNDAR, H. Et Al. (2011) . "Next generation sequencing in a family with infantile onset spinocerebellar ataxia identified a novel missense mutation in C10orf2 gene." European Human Genetics Conference , Amsterdam, Netherlands, p.11.

@conferencepaper{conferencepaper, author={HALİL DÜNDAR Et Al. }, title={Next generation sequencing in a family with infantile onset spinocerebellar ataxia identified a novel missense mutation in C10orf2 gene}, congress name={European Human Genetics Conference}, city={Amsterdam}, country={Netherlands}, year={2011}, pages={11} }