Matches in Wikidata for { <http://www.wikidata.org/entity/Q48613716> ?p ?o ?g. }
- Q48613716 description "2016 nî lūn-bûn" @default.
- Q48613716 description "2016年の論文" @default.
- Q48613716 description "2016年学术文章" @default.
- Q48613716 description "2016年学术文章" @default.
- Q48613716 description "2016年学术文章" @default.
- Q48613716 description "2016年学术文章" @default.
- Q48613716 description "2016年学术文章" @default.
- Q48613716 description "2016年学术文章" @default.
- Q48613716 description "2016年學術文章" @default.
- Q48613716 description "2016年學術文章" @default.
- Q48613716 description "2016年學術文章" @default.
- Q48613716 description "2016年學術文章" @default.
- Q48613716 description "2016年學術文章" @default.
- Q48613716 description "2016년 논문" @default.
- Q48613716 description "article científic" @default.
- Q48613716 description "article scientific" @default.
- Q48613716 description "article scientifique" @default.
- Q48613716 description "articol științific" @default.
- Q48613716 description "articolo scientifico" @default.
- Q48613716 description "artigo científico" @default.
- Q48613716 description "artigo científico" @default.
- Q48613716 description "artigo científico" @default.
- Q48613716 description "artikel ilmiah" @default.
- Q48613716 description "artikull shkencor" @default.
- Q48613716 description "artikulong pang-agham" @default.
- Q48613716 description "artykuł naukowy" @default.
- Q48613716 description "artículo científico publicado en 2016" @default.
- Q48613716 description "artículu científicu" @default.
- Q48613716 description "bilimsel makale" @default.
- Q48613716 description "bài báo khoa học" @default.
- Q48613716 description "naučni članak" @default.
- Q48613716 description "scienca artikolo" @default.
- Q48613716 description "scientific article published on 21 July 2016" @default.
- Q48613716 description "scientific article published on 21 July 2016" @default.
- Q48613716 description "scientific article published on 21 July 2016" @default.
- Q48613716 description "teaduslik artikkel" @default.
- Q48613716 description "tieteellinen artikkeli" @default.
- Q48613716 description "tudományos cikk" @default.
- Q48613716 description "vedecký článok" @default.
- Q48613716 description "vetenskaplig artikel" @default.
- Q48613716 description "videnskabelig artikel" @default.
- Q48613716 description "vitenskapelig artikkel" @default.
- Q48613716 description "vitskapeleg artikkel" @default.
- Q48613716 description "vědecký článek" @default.
- Q48613716 description "wetenschappelijk artikel" @default.
- Q48613716 description "wissenschaftlicher Artikel" @default.
- Q48613716 description "επιστημονικό άρθρο" @default.
- Q48613716 description "мақолаи илмӣ" @default.
- Q48613716 description "наукова стаття, опублікована в липні 2016" @default.
- Q48613716 description "научна статия" @default.
- Q48613716 description "научная статья" @default.
- Q48613716 description "научни чланак" @default.
- Q48613716 description "научни чланак" @default.
- Q48613716 description "מאמר מדעי" @default.
- Q48613716 description "مقالة علمية نشرت في 21 يوليو 2016" @default.
- Q48613716 description "২১ জুলাই ২০১৬-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ" @default.
- Q48613716 description "บทความทางวิทยาศาสตร์" @default.
- Q48613716 description "სამეცნიერო სტატია" @default.
- Q48613716 name "FKRP mutations, including a founder mutation, cause phenotype variability in Chinese patients with dystroglycanopathies." @default.
- Q48613716 name "FKRP mutations, including a founder mutation, cause phenotype variability in Chinese patients with dystroglycanopathies." @default.
- Q48613716 type Item @default.
- Q48613716 label "FKRP mutations, including a founder mutation, cause phenotype variability in Chinese patients with dystroglycanopathies." @default.
- Q48613716 label "FKRP mutations, including a founder mutation, cause phenotype variability in Chinese patients with dystroglycanopathies." @default.
- Q48613716 prefLabel "FKRP mutations, including a founder mutation, cause phenotype variability in Chinese patients with dystroglycanopathies." @default.
- Q48613716 prefLabel "FKRP mutations, including a founder mutation, cause phenotype variability in Chinese patients with dystroglycanopathies." @default.
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