Mishura S, Turchyna N, Heletiuk Y. A family case of hereditary olivopontocerebellar atrophy: features of diagnosis and course of the disease. USMYJ [Internet]. 2024Jun.27 [cited 2026Mar.21];146(2):23-0. Available from: https://mmj.nmuofficial.com/index.php/journal/article/view/393