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2012년 논문 مقالة علمية نشرت في 10 أكتوبر 2012 scientific article published on 10 October 2012 tudományos cikk 2012 nî lūn-bûn article scientifique научна статия наукова стаття, опублікована в жовтні 2012 vedecký článok videnskabelig artikel vitskapeleg artikkel artykuł naukowy 2012年论文 2012年論文 bilimsel makale научни чланак scientific article published on 10 October 2012 სამეცნიერო სტატია artikulong pang-agham naučni članak artículo científico publicado en 2012 vetenskaplig artikel 2012年论文 vitenskapelig artikkel επιστημονικό άρθρο 2012年論文 artigo científico научни чланак บทความทางวิทยาศาสตร์ מאמר מדעי articolo scientifico 2012 թվականի հոկտեմբերի 10-ին հրատարակված գիտական հոդված wetenschappelijk artikel 2012年の論文 научная статья artigo científico artículu científicu espublizáu en 2012 wissenschaftlicher Artikel 2012年论文 article científic teaduslik artikkel 2012年论文 2012年論文 scientific article published on 10 October 2012 vědecký článek 2012年论文 2012年論文 articol științific tieteellinen artikkeli artikull shkencor scienca artikolo ১০ অক্টোবর ২০১২-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ artikel ilmiah мақолаи илмӣ article scientific bài báo khoa học 2012年论文 2012年論文 artigo científico
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Wen-Ji Dong Tao Na Wei Zhang Guojin Wu Ji-Bin Peng
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Disease-causing R1185C mutation of WNK4 disrupts a regulatory mechanism involving calmodulin binding and SGK1 phosphorylation sites Disease-causing R1185C mutation of WNK4 disrupts a regulatory mechanism involving calmodulin binding and SGK1 phosphorylation sites Disease-causing R1185C mutation of WNK4 disrupts a regulatory mechanism involving calmodulin binding and SGK1 phosphorylation sites
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Disease-causing R1185C mutation of WNK4 disrupts a regulatory mechanism involving calmodulin binding and SGK1 phosphorylation sites Disease-causing R1185C mutation of WNK4 disrupts a regulatory mechanism involving calmodulin binding and SGK1 phosphorylation sites Disease-causing R1185C mutation of WNK4 disrupts a regulatory mechanism involving calmodulin binding and SGK1 phosphorylation sites
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Disease-causing R1185C mutation of WNK4 disrupts a regulatory mechanism involving calmodulin binding and SGK1 phosphorylation sites Disease-causing R1185C mutation of WNK4 disrupts a regulatory mechanism involving calmodulin binding and SGK1 phosphorylation sites Disease-causing R1185C mutation of WNK4 disrupts a regulatory mechanism involving calmodulin binding and SGK1 phosphorylation sites
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Disease-causing R1185C mutation of WNK4 disrupts a regulatory mechanism involving calmodulin binding and SGK1 phosphorylation sites
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