A novel NYX mutation associated with X-linked Congenital Stationary Night Blindness in a New Zealand family.

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dc.contributor.author Pradhan, M en
dc.contributor.author Sharp, D en
dc.contributor.author Mora, J en
dc.contributor.author Wittmer, M en
dc.contributor.author Berger, W en
dc.contributor.author Vincent, Andrea en
dc.date.accessioned 2012-03-12T02:22:13Z en
dc.date.issued 2011-03 en
dc.identifier.issn 1442-9071 en
dc.identifier.uri http://hdl.handle.net/2292/13853 en
dc.relation.ispartofseries J Clinical and Experimental Ophthalmology 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 A novel NYX mutation associated with X-linked Congenital Stationary Night Blindness in a New Zealand family. en
dc.type Journal Article en
dc.identifier.doi 10.4172/2155-9570.1000147 en
pubs.issue 4 en
pubs.volume 2 en
pubs.author-url http://www.omicsonline.org/2155-9570/2155-9570-2-147.php en
dc.rights.accessrights http://purl.org/eprint/accessRights/RestrictedAccess en
pubs.subtype Article en
pubs.elements-id 315742 en
pubs.org-id Medical and Health Sciences en
pubs.org-id School of Medicine en
pubs.org-id Ophthalmology Department en
pubs.number 147 en
pubs.record-created-at-source-date 2012-03-09 en


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