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2008년 논문 2008年論文 מאמר מדעי наукова стаття, опублікована в січні 2008 articolo scientifico scientific article artículu científicu espublizáu en 2008 artigo científico (publicado na 2008) บทความทางวิทยาศาสตร์ 2008年论文 2008 թուականի Յունուարին հրատարակուած գիտական յօդուած научна статия مقالهٔ علمی mokslinis straipsnis teaduslik artikkel 2008年论文 სამეცნიერო სტატია tudományos cikk vědecký článek научни чланак مقالة علمية scienca artikolo 2008 թվականի հունվարին հրատարակված գիտական հոդված artigo científico bài báo khoa học 2008年論文 2008年の論文 سائنسی مضمون vitskapeleg artikkel videnskabelig artikel (udgivet 2008) artykuł naukowy artikull shkencor 2008年论文 2008年論文 naučni članak articol științific научни чланак научная статья bilimsel makale ২০০৮-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ wetenschappelijk artikel 2008年论文 мақолаи илмӣ artículo científico publicado en 2008 2008 nî lūn-bûn article científic vitenskapelig artikkel vedecký článok tieteellinen artikkeli artigo científico (publicado na 2008) 2008年论文 article scientifique (publié 2008) 2008年論文 article scientific επιστημονικό άρθρο artikulong pang-agham 2008年论文 2008年論文 vetenskaplig artikel мақолаи илмӣ wissenschaftlicher Artikel
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Stefano Di Donato Claudia Cagnoli
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Spinocerebellar ataxia type 28: a novel autosomal dominant cerebellar ataxia characterized by slow progression and ophthalmoparesis. Spinocerebellar ataxia type 28: a novel autosomal dominant cerebellar ataxia characterized by slow progression and ophthalmoparesis. Spinocerebellar ataxia type 28: a novel autosomal dominant cerebellar ataxia characterized by slow progression and ophthalmoparesis.
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Spinocerebellar ataxia type 28: a novel autosomal dominant cerebellar ataxia characterized by slow progression and ophthalmoparesis. Spinocerebellar ataxia type 28: a novel autosomal dominant cerebellar ataxia characterized by slow progression and ophthalmoparesis. Spinocerebellar ataxia type 28: a novel autosomal dominant cerebellar ataxia characterized by slow progression and ophthalmoparesis.
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Spinocerebellar ataxia type 28: a novel autosomal dominant cerebellar ataxia characterized by slow progression and ophthalmoparesis. Spinocerebellar ataxia type 28: a novel autosomal dominant cerebellar ataxia characterized by slow progression and ophthalmoparesis. Spinocerebellar ataxia type 28: a novel autosomal dominant cerebellar ataxia characterized by slow progression and ophthalmoparesis.
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Spinocerebellar ataxia type 28: a novel autosomal dominant cerebellar ataxia characterized by slow progression and ophthalmoparesis
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