Novel OPN1LW/OPN1MW Exon 3 Haplotype-Associated Splicing Defect in Patients with X-Linked Cone Dysfunction

Stingl, Katarina; Baumann, Britta; De Angeli, Pietro; Vincent, Ajoy; Heon, Elise; Cordonnier, Monique; De Baere, Elfriede; Raskin, Salmo; Sato, Mario Teruo; Shiokawa, Naoye; Kohl, Susanne; Wissinger, Bernd

dc.contributor.author	Baumann, Britta
dc.contributor.author	De Angeli, Pietro
dc.contributor.author	Kohl, Susanne
dc.contributor.author	Wissinger, Bernd
dc.contributor.author	Štingl, Katarína
dc.date.accessioned	2022-11-07T08:57:18Z
dc.date.available	2022-11-07T08:57:18Z
dc.date.issued	2022
dc.identifier.issn	1422-0067
dc.identifier.uri	http://hdl.handle.net/10900/132843
dc.language.iso	en	de_DE
dc.publisher	Mdpi	de_DE
dc.relation.uri	http://dx.doi.org/10.3390/ijms23126868	de_DE
dc.subject.ddc	540	de_DE
dc.subject.ddc	570	de_DE
dc.title	Novel OPN1LW/OPN1MW Exon 3 Haplotype-Associated Splicing Defect in Patients with X-Linked Cone Dysfunction	de_DE
dc.type	Article	de_DE
utue.quellen.id	20220728000000_00575
utue.personen.roh	Stingl, Katarina
utue.personen.roh	Baumann, Britta
utue.personen.roh	De Angeli, Pietro
utue.personen.roh	Vincent, Ajoy
utue.personen.roh	Heon, Elise
utue.personen.roh	Cordonnier, Monique
utue.personen.roh	De Baere, Elfriede
utue.personen.roh	Raskin, Salmo
utue.personen.roh	Sato, Mario Teruo
utue.personen.roh	Shiokawa, Naoye
utue.personen.roh	Kohl, Susanne
utue.personen.roh	Wissinger, Bernd
dcterms.isPartOf.ZSTitelID	International Journal of Molecular Sciences	de_DE
dcterms.isPartOf.ZS-Issue	Article 6868	de_DE
dcterms.isPartOf.ZS-Volume	23 (12)	de_DE
utue.fakultaet	04 Medizinische Fakultät	de_DE