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artikull shkencor teaduslik artikkel სამეცნიერო სტატია مقالة علمية نشرت في 18 يونيو 2015 articolo scientifico vitskapeleg artikkel научна статия 2015年论文 наукова стаття, опублікована в червні 2015 artigo científico bài báo khoa học 2015年论文 vedecký článok מאמר מדעי 2015年論文 vitenskapelig artikkel 2015年论文 naučni članak 2015年の論文 ১৮ জুন ২০১৫-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ article scientifique 2015年論文 artikel ilmiah wissenschaftlicher Artikel 2015年论文 artículu científicu espublizáu en 2015 научни чланак scienca artikolo artykuł naukowy scientific article published on 18 June 2015 artikulong pang-agham artículo científico publicado en 2015 vědecký článek wetenschappelijk artikel บทความทางวิทยาศาสตร์ 2015년 논문 научная статья 2015年论文 artigo científico vetenskaplig artikel article scientific мақолаи илмӣ 2015年論文 2015 nî lūn-bûn 2015年论文 2015年論文 bilimsel makale επιστημονικό άρθρο 2015年論文 scientific article published on 18 June 2015 scientific article published on 18 June 2015 tudományos cikk article científic videnskabelig artikel tieteellinen artikkeli articol științific artigo científico научни чланак
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Jirair K Bedoyan Marisa W Friederich Orly Elpeleg Frédéric M Vaz Johan L K Van Hove Alberto Burlina Katherine Gowan Kathryn Chatfield Jos P N Ruiter Hans R Waterham Kaitlyn Bloom Michael J Bennett Megan K Dishop Renata C Gallagher
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Clinical and biochemical characterization of four patients with mutations in ECHS1. Clinical and biochemical characterization of four patients with mutations in ECHS1. Clinical and biochemical characterization of four patients with mutations in ECHS1.
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Clinical and biochemical characterization of four patients with mutations in ECHS1. Clinical and biochemical characterization of four patients with mutations in ECHS1. Clinical and biochemical characterization of four patients with mutations in ECHS1.
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Clinical and biochemical characterization of four patients with mutations in ECHS1. Clinical and biochemical characterization of four patients with mutations in ECHS1. Clinical and biochemical characterization of four patients with mutations in ECHS1.
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