Matches in Wikidata for { <http://www.wikidata.org/entity/Q54946696> ?p ?o ?g. }
- Q54946696 description "2011 nî lūn-bûn" @default.
- Q54946696 description "2011年の論文" @default.
- Q54946696 description "2011年学术文章" @default.
- Q54946696 description "2011年学术文章" @default.
- Q54946696 description "2011年学术文章" @default.
- Q54946696 description "2011年学术文章" @default.
- Q54946696 description "2011年学术文章" @default.
- Q54946696 description "2011年學術文章" @default.
- Q54946696 description "2011年學術文章" @default.
- Q54946696 description "2011年學術文章" @default.
- Q54946696 description "2011年學術文章" @default.
- Q54946696 description "2011年學術文章" @default.
- Q54946696 description "2011年學術文章" @default.
- Q54946696 description "2011년 논문" @default.
- Q54946696 description "article científic" @default.
- Q54946696 description "article scientific" @default.
- Q54946696 description "article scientifique (publié 2011)" @default.
- Q54946696 description "articol științific" @default.
- Q54946696 description "articolo scientifico" @default.
- Q54946696 description "artigo científico (publicado na 2011)" @default.
- Q54946696 description "artigo científico (publicado na 2011)" @default.
- Q54946696 description "artigo científico" @default.
- Q54946696 description "artikull shkencor" @default.
- Q54946696 description "artikulong pang-agham" @default.
- Q54946696 description "artykuł naukowy" @default.
- Q54946696 description "artículo científico publicado en 2011" @default.
- Q54946696 description "artículu científicu" @default.
- Q54946696 description "bilimsel makale" @default.
- Q54946696 description "bài báo khoa học" @default.
- Q54946696 description "mokslinis straipsnis" @default.
- Q54946696 description "naučni članak" @default.
- Q54946696 description "scienca artikolo" @default.
- Q54946696 description "scientific article" @default.
- Q54946696 description "teaduslik artikkel" @default.
- Q54946696 description "tieteellinen artikkeli" @default.
- Q54946696 description "tudományos cikk" @default.
- Q54946696 description "vedecký článok" @default.
- Q54946696 description "vetenskaplig artikel" @default.
- Q54946696 description "videnskabelig artikel (udgivet 2011)" @default.
- Q54946696 description "vitenskapelig artikkel" @default.
- Q54946696 description "vitskapeleg artikkel" @default.
- Q54946696 description "vědecký článek" @default.
- Q54946696 description "wetenschappelijk artikel" @default.
- Q54946696 description "wissenschaftlicher Artikel" @default.
- Q54946696 description "επιστημονικό άρθρο" @default.
- Q54946696 description "мақолаи илмӣ" @default.
- Q54946696 description "мақолаи илмӣ" @default.
- Q54946696 description "наукова стаття, опублікована у квітні 2011" @default.
- Q54946696 description "научна статия" @default.
- Q54946696 description "научная статья" @default.
- Q54946696 description "научни чланак" @default.
- Q54946696 description "научни чланак" @default.
- Q54946696 description "գիտական հոդված" @default.
- Q54946696 description "מאמר מדעי" @default.
- Q54946696 description "سائنسی مضمون" @default.
- Q54946696 description "مقالة علمية" @default.
- Q54946696 description "مقالهٔ علمی" @default.
- Q54946696 description "২০১১-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ" @default.
- Q54946696 description "บทความทางวิทยาศาสตร์" @default.
- Q54946696 description "სამეცნიერო სტატია" @default.
- Q54946696 name "Identification of p.A684V missense mutation in the WFS1 gene as a frequent cause of autosomal dominant optic atrophy and hearing impairment." @default.
- Q54946696 name "Identification of p.A684V missense mutation in the WFS1 gene as a frequent cause of autosomal dominant optic atrophy and hearing impairment." @default.
- Q54946696 type Item @default.
- Q54946696 label "Identification of p.A684V missense mutation in the WFS1 gene as a frequent cause of autosomal dominant optic atrophy and hearing impairment." @default.
- Q54946696 label "Identification of p.A684V missense mutation in the WFS1 gene as a frequent cause of autosomal dominant optic atrophy and hearing impairment." @default.
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- Q54946696 prefLabel "Identification of p.A684V missense mutation in the WFS1 gene as a frequent cause of autosomal dominant optic atrophy and hearing impairment." @default.
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