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scientific article 2013年学术文章 2013年の論文 مقالة علمية научни чланак articol științific מאמר מדעי article scientifique (publié 2013) 2013年學術文章 artykuł naukowy 2013年学术文章 2013年学术文章 научна статия artigo científico (publicado na 2013) 2013年學術文章 мақолаи илмӣ tieteellinen artikkeli vedecký článok article scientific articolo scientifico mokslinis straipsnis naučni članak 2013年学术文章 vetenskaplig artikel ২০১৩-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ vitskapeleg artikkel 2013年學術文章 գիտական հոդված мақолаи илмӣ 2013년 논문 article científic artikull shkencor artículo científico publicado en 2013 επιστημονικό άρθρο سائنسی مضمون vitenskapelig artikkel videnskabelig artikel (udgivet 2013) bilimsel makale სამეცნიერო სტატია 2013年学术文章 научная статья научни чланак vědecký článek artigo científico artigo científico (publicado na 2013) 2013年學術文章 مقالهٔ علمی 2013年學術文章 wissenschaftlicher Artikel wetenschappelijk artikel 2013 nî lūn-bûn tudományos cikk 2013年學術文章 scienca artikolo บทความทางวิทยาศาสตร์ artículu científicu teaduslik artikkel artikulong pang-agham наукова стаття, опублікована в лютому 2013 bài báo khoa học
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Ilham Ratbi Rick Kamps Isabel de Angst Abdelaziz Sefiani Jo van Oevelen Hubert Smeets Mike Gerards René de Coo Hans R Scholte Eveline Jongen Bianca van den Bosch Iris Boesten Bart de Koning Kees Schoonderwoerd Latifa Karim
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Exome sequencing reveals a novel Moroccan founder mutation in SLC19A3 as a new cause of early-childhood fatal Leigh syndrome Exome sequencing reveals a novel Moroccan founder mutation in SLC19A3 as a new cause of early-childhood fatal Leigh syndrome
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Exome sequencing reveals a novel Moroccan founder mutation in SLC19A3 as a new cause of early-childhood fatal Leigh syndrome Exome sequencing reveals a novel Moroccan founder mutation in SLC19A3 as a new cause of early-childhood fatal Leigh syndrome
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Exome sequencing reveals a novel Moroccan founder mutation in SLC19A3 as a new cause of early-childhood fatal Leigh syndrome Exome sequencing reveals a novel Moroccan founder mutation in SLC19A3 as a new cause of early-childhood fatal Leigh syndrome
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Exome sequencing reveals a novel Moroccan founder mutation in SLC19A3 as a new cause of early-childhood fatal Leigh syndrome
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Pt 3
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136
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