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наукова стаття, опублікована у квітні 2013 vědecký článek 2013 թվականի ապրիլին հրատարակված գիտական հոդված 2013年论文 tudományos cikk tieteellinen artikkeli επιστημονικό άρθρο artigo científico bài báo khoa học 2013年の論文 videnskabelig artikel (udgivet 2013) 2013年论文 научная статья vitenskapelig artikkel mokslinis straipsnis 2013年論文 2013年論文 article scientifique (publié 2013) artigo científico (publicado na 2013) 2013年論文 vitskapeleg artikkel wissenschaftlicher Artikel artikull shkencor სამეცნიერო სტატია wetenschappelijk artikel ২০১৩-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ 2013年论文 2013年论文 научни чланак artículu científicu espublizáu en 2013 scienca artikolo naučni članak scientific article articolo scientifico บทความทางวิทยาศาสตร์ 2013 nî lūn-bûn 2013년 논문 artículo científico publicado en 2013 teaduslik artikkel article científic מאמר מדעי 2013年論文 vetenskaplig artikel مقالة علمية 2013 թուականի Ապրիլին հրատարակուած գիտական յօդուած bilimsel makale мақолаи илмӣ научни чланак 2013年论文 2013年論文 научна статия мақолаи илмӣ سائنسی مضمون vedecký článok artykuł naukowy مقالهٔ علمی articol științific artikulong pang-agham 2013年论文 artigo científico (publicado na 2013) article scientific
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Lack of C9ORF72 coding mutations supports a gain of function for repeat expansions in amyotrophic lateral sclerosis Lack of C9ORF72 coding mutations supports a gain of function for repeat expansions in amyotrophic lateral sclerosis Lack of C9ORF72 coding mutations supports a gain of function for repeat expansions in amyotrophic lateral sclerosis
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Lack of C9ORF72 coding mutations supports a gain of function for repeat expansions in amyotrophic lateral sclerosis Lack of C9ORF72 coding mutations supports a gain of function for repeat expansions in amyotrophic lateral sclerosis Lack of C9ORF72 coding mutations supports a gain of function for repeat expansions in amyotrophic lateral sclerosis
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Lack of C9ORF72 coding mutations supports a gain of function for repeat expansions in amyotrophic lateral sclerosis Lack of C9ORF72 coding mutations supports a gain of function for repeat expansions in amyotrophic lateral sclerosis Lack of C9ORF72 coding mutations supports a gain of function for repeat expansions in amyotrophic lateral sclerosis
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