Hyperferritinaemia-cataract syndrome: worldwide mutations and phenotype of an increasingly diagnosed genetic disorder

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Bibliographische Detailangaben
Hauptverfasser: Millonig, Gunda (VerfasserIn) , Muckenthaler, Martina (VerfasserIn)
Dokumenttyp: Article (Journal) Buch/Monographie
Sprache:Englisch
Veröffentlicht: London [u.a.] Henry Stewart Publications 2016
Online-Zugang:Resolving-System, kostenfrei, Volltext: http://nbn-resolving.de/urn:nbn:de:bsz:16-heidok-201525
Volltext
Verfasserangaben:Gunda Millonig, Martina U. Muckenthaler, Sebastian Mueller

MARC

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