Ozcanyuz, D. G. Et Al. 2020. Dysarthria, Ataxia, and Dystonia Associated with COX20 (FAM36A) Gene Mutation: A Case Report of a Turkish Child. ANNALS OF INDIAN ACADEMY OF NEUROLOGY , vol.23, no.3 , 399-401.

Ozcanyuz, D. G., İNCECİK, F., Herguner, O. M., Mungan, N. O., & Bozdogan, S. T., (2020). Dysarthria, Ataxia, and Dystonia Associated with COX20 (FAM36A) Gene Mutation: A Case Report of a Turkish Child. ANNALS OF INDIAN ACADEMY OF NEUROLOGY , vol.23, no.3, 399-401.

Ozcanyuz, Duygu Et Al. "Dysarthria, Ataxia, and Dystonia Associated with COX20 (FAM36A) Gene Mutation: A Case Report of a Turkish Child," ANNALS OF INDIAN ACADEMY OF NEUROLOGY , vol.23, no.3, 399-401, 2020

Ozcanyuz, Duygu G. Et Al. "Dysarthria, Ataxia, and Dystonia Associated with COX20 (FAM36A) Gene Mutation: A Case Report of a Turkish Child." ANNALS OF INDIAN ACADEMY OF NEUROLOGY , vol.23, no.3, pp.399-401, 2020

Ozcanyuz, D. G. Et Al. (2020) . "Dysarthria, Ataxia, and Dystonia Associated with COX20 (FAM36A) Gene Mutation: A Case Report of a Turkish Child." ANNALS OF INDIAN ACADEMY OF NEUROLOGY , vol.23, no.3, pp.399-401.

@article{article, author={Duygu G. Ozcanyuz Et Al. }, title={Dysarthria, Ataxia, and Dystonia Associated with COX20 (FAM36A) Gene Mutation: A Case Report of a Turkish Child}, journal={ANNALS OF INDIAN ACADEMY OF NEUROLOGY}, year=2020, pages={399-401} }