A pathogenic haplotype, common in Europeans, causes autosomal recessive albinism and uncovers missing heritability in OCA1
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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2045-2322
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Anmerkungen
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online resource.
- Erschienen in
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A pathogenic haplotype, common in Europeans, causes autosomal recessive albinism and uncovers missing heritability in OCA1 ; volume:9 ; number:1 ; day:24 ; month:1 ; year:2019 ; pages:1-7 ; date:12.2019
Scientific reports ; 9, Heft 1 (24.1.2019), 1-7, 12.2019
- Urheber
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Grønskov, Karen
Jespersgaard, Cathrine
Bruun, Gitte Hoffmann
Harris, Pernille
Brøndum-Nielsen, Karen
Andresen, Brage S.
Rosenberg, Thomas
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
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10.1038/s41598-018-37272-5
- URN
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urn:nbn:de:101:1-2019022222543589551738
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
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14.08.2025, 10:50 MESZ
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Beteiligte
- Grønskov, Karen
- Jespersgaard, Cathrine
- Bruun, Gitte Hoffmann
- Harris, Pernille
- Brøndum-Nielsen, Karen
- Andresen, Brage S.
- Rosenberg, Thomas
- SpringerLink (Online service)
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