Deep-intronic variants in CNGB3 cause achromatopsia by pseudoexon activation

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dc.contributor.author Weisschuh, Nicole
dc.contributor.author Sturm, Marc
dc.contributor.author Baumann, Britta
dc.contributor.author Wissinger, Bernd
dc.contributor.author Kohl, Susanne
dc.contributor.author Štingl, Katarína
dc.date.accessioned 2020-11-09T09:26:42Z
dc.date.available 2020-11-09T09:26:42Z
dc.date.issued 2020
dc.identifier.issn 1098-1004
dc.identifier.uri http://hdl.handle.net/10900/109319
dc.language.iso en de_DE
dc.publisher Wiley de_DE
dc.relation.uri http://dx.doi.org/10.1002/humu.23920 de_DE
dc.subject.ddc 570 de_DE
dc.subject.ddc 610 de_DE
dc.title Deep-intronic variants in CNGB3 cause achromatopsia by pseudoexon activation de_DE
dc.type Article de_DE
utue.quellen.id 20200715072417_02435
utue.publikation.seiten 255-264 de_DE
utue.personen.roh Weisschuh, Nicole
utue.personen.roh Sturm, Marc
utue.personen.roh Baumann, Britta
utue.personen.roh Audo, Isabelle
utue.personen.roh Ayuso, Carmen
utue.personen.roh Bocquet, Beatrice
utue.personen.roh Branham, Kari
utue.personen.roh Brooks, Brian P.
utue.personen.roh Catala-Mora, Jaume
utue.personen.roh Giorda, Roberto
utue.personen.roh Heckenlively, John R.
utue.personen.roh Hufnagel, Robert B.
utue.personen.roh Jacobson, Samuel G.
utue.personen.roh Kellner, Ulrich
utue.personen.roh Kitsiou-Tzeli, Sofia
utue.personen.roh Matet, Alexandre
utue.personen.roh Sampol, Loreto Martorell
utue.personen.roh Meunier, Isabelle
utue.personen.roh Rudolph, Gunther
utue.personen.roh Sharon, Dror
utue.personen.roh Stingl, Katarina
utue.personen.roh Streubel, Berthold
utue.personen.roh Varsanyi, Balazs
utue.personen.roh Wissinger, Bernd
utue.personen.roh Kohl, Susanne
dcterms.isPartOf.ZSTitelID Human Mutation de_DE
dcterms.isPartOf.ZS-Issue 1 de_DE
dcterms.isPartOf.ZS-Volume 41 de_DE
utue.fakultaet 04 Medizinische Fakultät de_DE


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