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vetenskaplig artikel מאמר מדעי 2009년 논문 artículo científico publicado en 2009 artikull shkencor научна статия wetenschappelijk artikel bài báo khoa học mokslinis straipsnis مقالهٔ علمی 2009年学术文章 scienca artikolo article scientific articolo scientifico article científic vitskapeleg artikkel 2009年学术文章 tudományos cikk 2009年學術文章 научни чланак 2009年學術文章 научни чланак سائنسی مضمون artigo científico (publicado na 2009) სამეცნიერო სტატია teaduslik artikkel наукова стаття, опублікована в червні 2009 artigo científico (publicado na 2009) 2009年學術文章 2009年の論文 գիտական հոդված artikulong pang-agham научная статья wissenschaftlicher Artikel bilimsel makale tieteellinen artikkeli vitenskapelig artikkel 2009年学术文章 επιστημονικό άρθρο мақолаи илмӣ article scientifique (publié 2009) scientific article 2009年學術文章 2009年學術文章 مقالة علمية 2009 nî lūn-bûn vědecký článek vedecký článok мақолаи илмӣ videnskabelig artikel (udgivet 2009) naučni članak articol științific artículu científicu 2009年学术文章 ২০০৯-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ บทความทางวิทยาศาสตร์ 2009年学术文章 2009年學術文章 artykuł naukowy artigo científico
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2009-06-07T00:00:00Z
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Gerrit Jansen Bluma Berman Fabian Glaser Inbal Lasry
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Hereditary folate malabsorption: a positively charged amino acid at position 113 of the proton-coupled folate transporter Hereditary folate malabsorption: a positively charged amino acid at position 113 of the proton-coupled folate transporter (PCFT/SLC46A1) is required for folic acid binding.
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Hereditary folate malabsorption: a positively charged amino acid at position 113 of the proton-coupled folate transporter Hereditary folate malabsorption: a positively charged amino acid at position 113 of the proton-coupled folate transporter (PCFT/SLC46A1) is required for folic acid binding.
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Hereditary folate malabsorption: a positively charged amino acid at position 113 of the proton-coupled folate transporter (PCFT/SLC46A1) is required for folic acid binding. Hereditary folate malabsorption: a positively charged amino acid at position 113 of the proton-coupled folate transporter
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Hereditary folate malabsorption: a positively charged amino acid at position 113 of the proton-coupled folate transporter (PCFT/SLC46A1) is required for folic acid binding.
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10.1016/J.BBRC.2009.06.007