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tieteellinen artikkeli наукова стаття, опублікована в грудні 2008 articolo scientifico (pubblicato il 2008-12) artículu científicu espublizáu en 2008 2008年論文 ശാസ്ത്ര പ്രബന്ധം artículo científico publicado en 2008 vitenskapelig artikkel wetenschappelijk artikel (gepubliceerd op 2008-12) научни чланак scientific article 2008年論文 vitskapeleg artikkel wissenschaftlicher Artikel (veröffentlicht in Dezember 2008) 2008年论文 επιστημονικό άρθρο مقالة علمية (نشرت في ديسمبر 2008) articol științific mokslinis straipsnis vedecký článok (publikovaný 2008-12) artikulong pang-agham บทความทางวิทยาศาสตร์ мақолаи илмӣ artigo científico (publicado na 2008) 2008年论文 2008年論文 научна статия artykuł naukowy vetenskaplig artikel научни чланак (објављен 2008-12) 2008年論文 2008年论文 scienca artikolo article scientific naučni članak מאמר מדעי 2008년 논문 2008 nî lūn-bûn 2008年论文 article scientifique (publié 2008-12) مقالهٔ علمی article científic bilimsel makale ২০০৮-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ 2008年の論文 2008年论文 vědecký článek publikovaný v roce 2008 سائنسی مضمون tudományos cikk artigo científico (publicado na 2008-12) სამეცნიერო სტატია мақолаи илмӣ videnskabelig artikel (udgivet 2008-12) научная статья artikull shkencor 2008 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած bài báo khoa học teaduslik artikkel 2008年論文 2008年论文 artigo científico 2008 թվականի դեկտեմբերին հրատարակված գիտական հոդված
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Jessica M Vanslambrouck John E J Rasko Sonja Kowalczuk Stefan Bröer Cynthia Ng Juleen A Cavanaugh Christiane Auray-Blais Angelika Bröer Helen Rodgers
rdfs:label
Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters
skos:prefLabel
Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters
schema:name
Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters
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Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters
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