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naučni članak artigo científico 2013年學術文章 мақолаи илмӣ tudományos cikk bilimsel makale articolo scientifico artículu científicu espublizáu en 2013 научни чланак articol științific vitskapeleg artikkel tieteellinen artikkeli vetenskaplig artikel scientific article artículo científico publicado en 2013 article científic 2013 nî lūn-bûn artikull shkencor 2013年學術文章 article scientifique (publié 2013) научни чланак mokslinis straipsnis مقالهٔ علمی научна статия 2013年学术文章 מאמר מדעי سائنسی مضمون 2013年學術文章 2013年學術文章 artigo científico (publicado na 2013) 2013年学术文章 videnskabelig artikel (udgivet 2013) επιστημονικό άρθρο мақолаи илмӣ wetenschappelijk artikel ২০১৩-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ 2013年学术文章 2013년 논문 บทความทางวิทยาศาสตร์ article scientific bài báo khoa học artikulong pang-agham գիտական հոդված 2013年學術文章 vědecký článek научная статья teaduslik artikkel სამეცნიერო სტატია scienca artikolo wissenschaftlicher Artikel vedecký článok 2013年の論文 2013年學術文章 artigo científico (publicado na 2013) مقالة علمية наукова стаття, опублікована в березні 2013 2013年学术文章 artykuł naukowy 2013年学术文章 vitenskapelig artikkel
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Mats I Nilsson Munim Saeed Marissa L Laureano
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Dysferlin aggregation in limb-girdle muscular dystrophy type 2B/Miyoshi Myopathy necessitates mutational screen for diagnosis [corrected]. Dysferlin aggregation in limb-girdle muscular dystrophy type 2B/Miyoshi Myopathy necessitates mutational screen for diagnosis [corrected].
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Dysferlin aggregation in limb-girdle muscular dystrophy type 2B/Miyoshi Myopathy necessitates mutational screen for diagnosis [corrected]. Dysferlin aggregation in limb-girdle muscular dystrophy type 2B/Miyoshi Myopathy necessitates mutational screen for diagnosis [corrected].
schema:name
Dysferlin aggregation in limb-girdle muscular dystrophy type 2B/Miyoshi Myopathy necessitates mutational screen for diagnosis [corrected]. Dysferlin aggregation in limb-girdle muscular dystrophy type 2B/Miyoshi Myopathy necessitates mutational screen for diagnosis [corrected].
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Dysferlin aggregation in limb-girdle muscular dystrophy type 2B/Miyoshi Myopathy necessitates mutational screen for diagnosis [corrected].
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10.1002/MUS.23666
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