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A novel homozygous truncating GNAT1 mutation implicated in retinal degeneration
- Correspondence to Dr Matthew Carrigan, Smurfit Institute of Genetics, Trinity College Dublin, College Green, Dublin 2, Ireland; carrigma{at}tcd.ie
Citation
A novel homozygous truncating GNAT1 mutation implicated in retinal degeneration
Publication history
- Received March 27, 2015
- Revised July 9, 2015
- Accepted August 1, 2015
- First published October 15, 2015.
Online issue publication
March 22, 2016
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Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/ This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/