A deep intronic substitution in CNGB3 is one of the major causes of achromatopsia among Jewish patients

Aweidah, Hamzah; Salameh, Manar; Yahalom, Claudia; Blumenfeld, Anat; Macarov, Michal; Weisschuh, Nicole; Kohl, Susanne; Banin, Eyal; Sharon, Dror

dc.contributor.author	Weisschuh, Nicole
dc.contributor.author	Kohl, Susanne
dc.date.accessioned	2022-08-02T08:01:44Z
dc.date.available	2022-08-02T08:01:44Z
dc.date.issued	2021
dc.identifier.issn	1090-0535
dc.identifier.uri	http://hdl.handle.net/10900/129838
dc.language.iso	en	en
dc.publisher	Molecular Vision	de_DE
dc.relation.uri	http://doi.org/10.1002/humu.23920	de_DE
dc.subject.ddc	570	de_DE
dc.subject.ddc	610	de_DE
dc.title	A deep intronic substitution in CNGB3 is one of the major causes of achromatopsia among Jewish patients	de_DE
dc.type	Article	de_DE
utue.quellen.id	20211125174918_00564
utue.publikation.seiten	588-600	de_DE
utue.personen.roh	Aweidah, Hamzah
utue.personen.roh	Salameh, Manar
utue.personen.roh	Yahalom, Claudia
utue.personen.roh	Blumenfeld, Anat
utue.personen.roh	Macarov, Michal
utue.personen.roh	Weisschuh, Nicole
utue.personen.roh	Kohl, Susanne
utue.personen.roh	Banin, Eyal
utue.personen.roh	Sharon, Dror
dcterms.isPartOf.ZSTitelID	Molecular Vision	de_DE
dcterms.isPartOf.ZS-Volume	27	de_DE
utue.fakultaet	04 Medizinische Fakultät