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- Q61444610 description "article publié dans la revue scientifique Scientific Reports" @default.
- Q61444610 description "artículu científicu" @default.
- Q61444610 description "bài báo khoa học" @default.
- Q61444610 description "im Januar 2019 veröffentlichter wissenschaftlicher Artikel" @default.
- Q61444610 description "scientific article published in Scientific Reports" @default.
- Q61444610 description "wetenschappelijk artikel" @default.
- Q61444610 description "наукова стаття, опублікована в січні 2019" @default.
- Q61444610 name "A pathogenic haplotype, common in Europeans, causes autosomal recessive albinism and uncovers missing heritability in OCA1" @default.
- Q61444610 name "A pathogenic haplotype, common in Europeans, causes autosomal recessive albinism and uncovers missing heritability in OCA1" @default.
- Q61444610 type Item @default.
- Q61444610 label "A pathogenic haplotype, common in Europeans, causes autosomal recessive albinism and uncovers missing heritability in OCA1" @default.
- Q61444610 label "A pathogenic haplotype, common in Europeans, causes autosomal recessive albinism and uncovers missing heritability in OCA1" @default.
- Q61444610 prefLabel "A pathogenic haplotype, common in Europeans, causes autosomal recessive albinism and uncovers missing heritability in OCA1" @default.
- Q61444610 prefLabel "A pathogenic haplotype, common in Europeans, causes autosomal recessive albinism and uncovers missing heritability in OCA1" @default.
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- Q61444610 P1476 "A pathogenic haplotype, common in Europeans, causes autosomal recessive albinism and uncovers missing heritability in OCA1" @default.
- Q61444610 P2093 "Cathrine Jespersgaard" @default.
- Q61444610 P2093 "Gitte Hoffmann Bruun" @default.
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