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2012年の論文 bài báo khoa học գիտական հոդված ২০১২-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ videnskabelig artikel (udgivet 2012) tieteellinen artikkeli artigo científico мақолаи илмӣ scienca artikolo vetenskaplig artikel artículo científico publicado en 2012 2012年论文 artigo científico (publicado na 2012) научная статья מאמר מדעי vedecký článok επιστημονικό άρθρο مقالهٔ علمی سائنسی مضمون bilimsel makale 2012年论文 artículu científicu espublizáu en 2012 2012年論文 vitskapeleg artikkel article scientific wissenschaftlicher Artikel artykuł naukowy artikulong pang-agham articol științific 2012年论文 2012年論文 บทความทางวิทยาศาสตร์ 2012年論文 vědecký článek article scientifique (publié 2012) научни чланак vitenskapelig artikkel articolo scientifico სამეცნიერო სტატია naučni članak mokslinis straipsnis 2012 nî lūn-bûn 2012년 논문 научни чланак tudományos cikk article científic 2012年论文 teaduslik artikkel 2012年論文 2012年论文 artigo científico (publicado na 2012) научна статия 2012年论文 wetenschappelijk artikel 2012年論文 مقالة علمية نشرت بتاريخ 18-7-2012 наукова стаття, опублікована в липні 2012 scientific article мақолаи илмӣ artikull shkencor
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Chromosome 4q25 variants are genetic modifiers of rare ion channel mutations associated with familial atrial fibrillation Chromosome 4q25 variants are genetic modifiers of rare ion channel mutations associated with familial atrial fibrillation Chromosome 4q25 variants are genetic modifiers of rare ion channel mutations associated with familial atrial fibrillation
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Chromosome 4q25 variants are genetic modifiers of rare ion channel mutations associated with familial atrial fibrillation Chromosome 4q25 variants are genetic modifiers of rare ion channel mutations associated with familial atrial fibrillation Chromosome 4q25 variants are genetic modifiers of rare ion channel mutations associated with familial atrial fibrillation
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Chromosome 4q25 variants are genetic modifiers of rare ion channel mutations associated with familial atrial fibrillation Chromosome 4q25 variants are genetic modifiers of rare ion channel mutations associated with familial atrial fibrillation Chromosome 4q25 variants are genetic modifiers of rare ion channel mutations associated with familial atrial fibrillation
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