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২০১২-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ 2012年論文 سائنسی مضمون 2012년 논문 2012年論文 2012年论文 artigo científico wetenschappelijk artikel artigo científico (publicado na 2012) мақолаи илмӣ מאמר מדעי scienca artikolo 2012 nî lūn-bûn vitenskapelig artikkel 2012年论文 2012 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած artículu científicu espublizáu en 2012 bài báo khoa học tieteellinen artikkeli наукова стаття, опублікована в листопаді 2012 2012年論文 2012年论文 vitskapeleg artikkel 2012年论文 научная статья სამეცნიერო სტატია videnskabelig artikel (udgivet 2012) artikulong pang-agham articol științific vetenskaplig artikel artykuł naukowy мақолаи илмӣ 2012年論文 научни чланак vědecký článek 2012 թվականի նոյեմբերին հրատարակված գիտական հոդված научни чланак wissenschaftlicher Artikel bilimsel makale naučni članak article scientific artigo científico (publicado na 2012) artículo científico publicado en 2012 2012年論文 2012年论文 article scientifique (publié 2012) articolo scientifico vedecký článok tudományos cikk 2012年の論文 บทความทางวิทยาศาสตร์ научна статия artikull shkencor 2012年论文 مقالهٔ علمی مقالة علمية scientific article mokslinis straipsnis επιστημονικό άρθρο article científic teaduslik artikkel
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Lynn Sanford Eleanna Kara Henry H Houlden Esther Meyer Elisabeth Graf
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Exome sequencing reveals de novo WDR45 mutations causing a phenotypically distinct, X-linked dominant form of NBIA. Exome sequencing reveals de novo WDR45 mutations causing a phenotypically distinct, X-linked dominant form of NBIA. Exome sequencing reveals de novo WDR45 mutations causing a phenotypically distinct, X-linked dominant form of NBIA.
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Exome sequencing reveals de novo WDR45 mutations causing a phenotypically distinct, X-linked dominant form of NBIA. Exome sequencing reveals de novo WDR45 mutations causing a phenotypically distinct, X-linked dominant form of NBIA. Exome sequencing reveals de novo WDR45 mutations causing a phenotypically distinct, X-linked dominant form of NBIA.
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Exome sequencing reveals de novo WDR45 mutations causing a phenotypically distinct, X-linked dominant form of NBIA. Exome sequencing reveals de novo WDR45 mutations causing a phenotypically distinct, X-linked dominant form of NBIA. Exome sequencing reveals de novo WDR45 mutations causing a phenotypically distinct, X-linked dominant form of NBIA.
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