CNGB3 mutation spectrum including copy number variations in 552 achromatopsia patients

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	Article	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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