Homozygous missense variant in the human CNGA3 channel causes cone-rod dystrophy

Shaikh, Rehan S.; Reuter, Peggy; Sisk, Robert A.; Kausar, Tasleem; Shahzad, Mohsin; Maqsood, Muhammad I.; Yousif, Ateeq; Ali, Muhammad; Riazuddin, Saima; Wissinger, Bernd; Ahmed, Zubair M.

dc.contributor.author	Reuter, Peggy
dc.contributor.author	Wissinger, Bernd
dc.date.accessioned	2015-11-17T09:28:37Z
dc.date.available	2015-11-17T09:28:37Z
dc.date.issued	2015
dc.identifier.issn	1018-4813
dc.identifier.uri	http://hdl.handle.net/10900/66516
dc.language.iso	en	en
dc.publisher	Nature Publishing Group	de_DE
dc.relation.uri	http://dx.doi.org/10.1038/ejhg.2014.136
dc.rights	info:eu-repo/semantics/closedAccess
dc.subject.ddc	570	de_DE
dc.subject.ddc	610	de_DE
dc.title	Homozygous missense variant in the human CNGA3 channel causes cone-rod dystrophy	de_DE
dc.type	Article	de_DE
utue.quellen.id	20150901145020_01214
utue.publikation.seiten	473-480	de_DE
utue.personen.roh	Shaikh, Rehan S.
utue.personen.roh	Reuter, Peggy
utue.personen.roh	Sisk, Robert A.
utue.personen.roh	Kausar, Tasleem
utue.personen.roh	Shahzad, Mohsin
utue.personen.roh	Maqsood, Muhammad I.
utue.personen.roh	Yousif, Ateeq
utue.personen.roh	Ali, Muhammad
utue.personen.roh	Riazuddin, Saima
utue.personen.roh	Wissinger, Bernd
utue.personen.roh	Ahmed, Zubair M.
dcterms.isPartOf.ZSTitelID	European Journal of Human Genetics	de_DE
dcterms.isPartOf.ZS-Issue	4	de_DE
dcterms.isPartOf.ZS-Volume	23	de_DE
utue.fakultaet	04 Medizinische Fakultät