CNGB3 mutation spectrum including copy number variations in 552 achromatopsia patients

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dc.contributor.author Mayer, Anja K en
dc.contributor.author Van Cauwenbergh, Caroline en
dc.contributor.author Rother, Christine en
dc.contributor.author Baumann, Britta en
dc.contributor.author Reuter, Peggy en
dc.contributor.author De Baere, Elfride en
dc.contributor.author Wissinger, Bernd en
dc.contributor.author Kohl, Susanne en
dc.date.accessioned 2018-10-02T21:30:06Z en
dc.date.issued 2017-11 en
dc.identifier.issn 1059-7794 en
dc.identifier.uri http://hdl.handle.net/2292/38272 en
dc.relation.ispartofseries Human Mutation en
dc.rights Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated. Previously published items are made available in accordance with the copyright policy of the publisher. en
dc.rights.uri https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm en
dc.title CNGB3 mutation spectrum including copy number variations in 552 achromatopsia patients en
dc.type Journal Article en
dc.identifier.doi 10.1002/humu.23311 en
pubs.issue 11 en
pubs.begin-page 1579 en
pubs.volume 38 en
dc.rights.holder Copyright: The author en
pubs.end-page 1591 en
pubs.publication-status Published en
dc.rights.accessrights http://purl.org/eprint/accessRights/RestrictedAccess en
pubs.elements-id 697219 en
pubs.org-id Medical and Health Sciences en
pubs.org-id School of Medicine en
pubs.org-id Ophthalmology Department en
pubs.online-publication-date 2017-08-28 en


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