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

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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 Artikel 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


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