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artigo científico article scientifique publié en 2013 სამეცნიერო სტატია artigo científico (publicado na 2013) 2013年學術文章 мақолаи илмӣ مقالهٔ علمی artikull shkencor teaduslik artikkel videnskabelig artikel (udgivet 2013) bilimsel makale vitskapeleg artikkel научна статия vetenskaplig artikel vědecký článek 2013年學術文章 wissenschaftlicher Artikel מאמר מדעי wetenschappelijk artikel 2013年学术文章 научни чланак mokslinis straipsnis article científic 2013年の論文 naučni članak 2013년 논문 vitenskapelig artikkel 2013年學術文章 article scientific scienca artikolo บทความทางวิทยาศาสตร์ artículu científicu espublizáu en 2013 գիտական հոդված 2013年学术文章 tieteellinen artikkeli επιστημονικό άρθρο 2013年學術文章 scientific article published on 06 June 2013 bài báo khoa học سائنسی مضمون наукова стаття, опублікована в червні 2013 articolo scientifico artykuł naukowy vedecký článok 2013年学术文章 научни чланак artigo científico (publicado na 2013) ২০১৩-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ tudományos cikk artikulong pang-agham 2013年学术文章 научная статья artículo científico publicado en 2013 2013年學術文章 articol științific 2013年学术文章 мақолаи илмӣ 2013 nî lūn-bûn 2013年學術文章 مقالة علمية نشرت في 06 يونيو 2013
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Goknur Haliloglu Lindsay C Swanson Satoko Miyatake Eriko Koshimizu Masaaki Shiina Shintaro Imamura Michiaki Yamashita Ekkhard Willichowski Pauliina Vornanen Beril Talim Gulsev Kale Takashi Ohya Emily J Todd Victoria A Fabian Naomichi Matsumoto Norma B Romero Yuko Sakamoto Diclehan Orhan Nina Kresoje Mark R Davis Inger E Silberg Caroline A Sewry Kyle S Yau Cathy Kiraly-Borri Carina Wallgren-Pettersson Yoram Nevo Francesco Muntoni Noriko Miyake Hiroshi Doi Hitoshi Osaka Ozge Ceyhan Gianina Ravenscroft Padma Sivadorai Helge Amthor Kazuhiro Ogata Sumimasa Yamashita Yukiko K Hayashi Adnan Manzur
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Mutations in KLHL40 are a frequent cause of severe autosomal-recessive nemaline myopathy Mutations in KLHL40 are a frequent cause of severe autosomal-recessive nemaline myopathy Mutations in KLHL40 are a frequent cause of severe autosomal-recessive nemaline myopathy
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Mutations in KLHL40 are a frequent cause of severe autosomal-recessive nemaline myopathy Mutations in KLHL40 are a frequent cause of severe autosomal-recessive nemaline myopathy Mutations in KLHL40 are a frequent cause of severe autosomal-recessive nemaline myopathy
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Mutations in KLHL40 are a frequent cause of severe autosomal-recessive nemaline myopathy Mutations in KLHL40 are a frequent cause of severe autosomal-recessive nemaline myopathy Mutations in KLHL40 are a frequent cause of severe autosomal-recessive nemaline myopathy
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Mutations in KLHL40 are a frequent cause of severe autosomal-recessive nemaline myopathy
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