TÜRKDOĞAN, D. Et Al. 2024. The First Case of Autosomal Recessive Cerebellar Ataxia with Prominent Paroxysmal Non-kinesigenic Dyskinesia Caused by a Truncating FGF14 Variant in a Turkish Patient. Movement Disorders .

TÜRKDOĞAN, D., Smolina, N., Tekgül, Ş., Gül, T., Yeşilyurt, A., Houlden, H., ... Zuchner, S.(2024). The First Case of Autosomal Recessive Cerebellar Ataxia with Prominent Paroxysmal Non-kinesigenic Dyskinesia Caused by a Truncating FGF14 Variant in a Turkish Patient. Movement Disorders .

TÜRKDOĞAN, DİLŞAD Et Al. "The First Case of Autosomal Recessive Cerebellar Ataxia with Prominent Paroxysmal Non-kinesigenic Dyskinesia Caused by a Truncating FGF14 Variant in a Turkish Patient," Movement Disorders , 2024

TÜRKDOĞAN, DİLŞAD Et Al. "The First Case of Autosomal Recessive Cerebellar Ataxia with Prominent Paroxysmal Non-kinesigenic Dyskinesia Caused by a Truncating FGF14 Variant in a Turkish Patient." Movement Disorders , 2024

TÜRKDOĞAN, D. Et Al. (2024) . "The First Case of Autosomal Recessive Cerebellar Ataxia with Prominent Paroxysmal Non-kinesigenic Dyskinesia Caused by a Truncating FGF14 Variant in a Turkish Patient." Movement Disorders .

@article{article, author={DİLŞAD TÜRKDOĞAN Et Al. }, title={The First Case of Autosomal Recessive Cerebellar Ataxia with Prominent Paroxysmal Non-kinesigenic Dyskinesia Caused by a Truncating FGF14 Variant in a Turkish Patient}, journal={Movement Disorders}, year=2024}