Orthopaedic phenotyping of NGLY1 deficiency using an international, family-led disease registry
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1750-1172
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Anmerkungen
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online resource.
- Erschienen in
-
Orthopaedic phenotyping of NGLY1 deficiency using an international, family-led disease registry ; volume:14 ; number:1 ; day:19 ; month:6 ; year:2019 ; pages:1-8 ; date:12.2019
Orphanet journal of rare diseases ; 14, Heft 1 (19.6.2019), 1-8, 12.2019
- Urheber
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Cahan, Eli M.
Frick, Steven L.
- Beteiligte Personen und Organisationen
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SpringerLink (Online service)
- DOI
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10.1186/s13023-019-1131-4
- URN
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urn:nbn:de:101:1-2019091114165666949645
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:27 MESZ
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Beteiligte
- Cahan, Eli M.
- Frick, Steven L.
- SpringerLink (Online service)
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