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PDFLaboratory science
ND4L gene concurrent 10609T>C and 10663T>C mutations are associated with Leber's hereditary optic neuropathy in a large pedigree from Kuwait
- Correspondence to Dr Osama Alsmadi, Dasman Genome Centre, Dasman Institute, PO Box 1180, Dasman 15462, Kuwait; osama.alsmadi{at}dasmaninstitute.org or oalsmadi{at}gmail.com
Citation
ND4L gene concurrent 10609T>C and 10663T>C mutations are associated with Leber's hereditary optic neuropathy in a large pedigree from Kuwait
Publication history
- Received August 6, 2013
- Revised January 12, 2014
- Accepted February 3, 2014
- First published February 25, 2014.
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://group.bmj.com/group/rights-licensing/permissions This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 3.0) 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/3.0/