Açık Akademik Arşiv Sistemi

Browsing Makale Koleksiyonu by Author "Sayan, S; Kotan, D; Gundogdu-Eken, A; Sahbaz, I; Kocoglu, C; Basak, AN;"

Browsing Makale Koleksiyonu by Author "Sayan, S; Kotan, D; Gundogdu-Eken, A; Sahbaz, I; Kocoglu, C; Basak, AN;"

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  • Phenotypic and Genotypic Analysis of Hereditary Ataxia Patients in Sakarya City, Turkey 
    Saadet Sayan; Dilcan Kotan; Kotan Dündar, Dilcan; Asli Gundogdu-Eken; Irmak Sahbaz; Cemile Kocoglu; A. Nazli Basak (AVES, 2019)
    Conclusion: Hereditary ataxias are rare neurodegenerative disorders. Large genetic pool, ethnic and local differences complicate diagnosing even further. Our study contributes to the literature by reflecting phenotypic and ...