Loss of HCN1 enhances disease progression in mouse models of CNG channel-linked retinitis pigmentosa and achromatopsia

Schoen, Christian; Asteriti, Sabrina; Koch, Susanne; Sothilingam, Vithiyanjali; Garrido, Marina Garcia; Tanimoto, Naoyuki; Herms, Jochen; Seeliger, Mathias W.; Cangiano, Lorenzo; Biel, Martin; Michalakis, Stylianos

dc.contributor.author	Sothilingam, Vithiyanjali
dc.contributor.author	Garcia Garrido, Marina
dc.contributor.author	Tanimoto, Naoyuki
dc.contributor.author	Seeliger, Wolfgang Mathias
dc.date.accessioned	2017-03-15T15:57:17Z
dc.date.available	2017-03-15T15:57:17Z
dc.date.issued	2016
dc.identifier.issn	1460-2083
dc.identifier.uri	http://hdl.handle.net/10900/75104
dc.language.iso	en	en
dc.publisher	Oxford Univ Press	de_DE
dc.relation.uri	http://dx.doi.org/10.1093/hmg/ddv639
dc.rights	info:eu-repo/semantics/closedAccess
dc.subject.ddc	570	de_DE
dc.subject.ddc	610	de_DE
dc.title	Loss of HCN1 enhances disease progression in mouse models of CNG channel-linked retinitis pigmentosa and achromatopsia	de_DE
dc.type	Article	de_DE
utue.quellen.id	20160915142648_01297
utue.publikation.seiten	1165-1175	de_DE
utue.personen.roh	Schoen, Christian
utue.personen.roh	Asteriti, Sabrina
utue.personen.roh	Koch, Susanne
utue.personen.roh	Sothilingam, Vithiyanjali
utue.personen.roh	Garrido, Marina Garcia
utue.personen.roh	Tanimoto, Naoyuki
utue.personen.roh	Herms, Jochen
utue.personen.roh	Seeliger, Mathias W.
utue.personen.roh	Cangiano, Lorenzo
utue.personen.roh	Biel, Martin
utue.personen.roh	Michalakis, Stylianos
dcterms.isPartOf.ZSTitelID	Human Molecular Genetics	de_DE
dcterms.isPartOf.ZS-Issue	6	de_DE
dcterms.isPartOf.ZS-Volume	25	de_DE
utue.fakultaet	04 Medizinische Fakultät