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Mutations in PCDH21 cause autosomal recessive cone-rod dystrophy
- Correspondence to Elsebet Ostergaard, Department of Clinical Genetics 4062, National University Hospital Rigshospitalet, Blegdamsvej 9, Copenhagen 2100, Denmark; elsebet.ostergaard{at}dadlnet.dk
Citation
Mutations in PCDH21 cause autosomal recessive cone-rod dystrophy
Publication history
- Received May 21, 2009
- Revised December 19, 2009
- Accepted January 14, 2010
- First published August 30, 2010.
Online issue publication
July 29, 2016
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© 2010, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions. This is an open-access article distributed under the terms of the Creative Commons Attribution Non-commercial License, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited, the use is non commercial and is otherwise in compliance with the license. See: http://creativecommons.org/licenses/by-nc/2.0/ and http://creativecommons.org/licenses/by-nc/2.0/legalcode.