CNGB3 mutation spectrum including copy number variations in 552 achromatopsia patients

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dc.contributor.author Rother, Christine
dc.contributor.author Baumann, Britta
dc.contributor.author Reuter, Peggy
dc.contributor.author Wissinger, Bernd
dc.contributor.author Kohl, Susanne
dc.contributor.author Mayer, Anja Kathrin
dc.date.accessioned 2019-04-23T07:59:47Z
dc.date.available 2019-04-23T07:59:47Z
dc.date.issued 2017
dc.identifier.issn 1098-1004
dc.identifier.uri http://hdl.handle.net/10900/87901
dc.language.iso en de_DE
dc.publisher Wiley de_DE
dc.relation.uri http://dx.doi.org/10.1002/humu.23311 de_DE
dc.rights info:eu-repo/semantics/closedAccess
dc.subject.ddc 570 de_DE
dc.subject.ddc 610 de_DE
dc.title CNGB3 mutation spectrum including copy number variations in 552 achromatopsia patients de_DE
dc.type Artikel de_DE
utue.quellen.id 20190131163842_00645
utue.publikation.seiten 1579-1591 de_DE
utue.personen.roh Mayer, Anja K.
utue.personen.roh Van Cauwenbergh, Caroline
utue.personen.roh Rother, Christine
utue.personen.roh Baumann, Britta
utue.personen.roh Reuter, Peggy
utue.personen.roh De Baere, Elfride
utue.personen.roh Wissinger, Bernd
utue.personen.roh Kohl, Susanne
dcterms.isPartOf.ZSTitelID Human Mutation de_DE
dcterms.isPartOf.ZS-Issue 11 de_DE
dcterms.isPartOf.ZS-Volume 38 de_DE
utue.fakultaet 04 Medizinische Fakultät de_DE


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