Article info
Clinical science
Congenital monocular elevation deficiency associated with a novel TUBB3 gene variant
- Correspondence to Dr Mervyn G Thomas, Ulverscroft Eye Unit, Department of Neuroscience, Psychology and Behaviour, University of Leicester, Leicester LE1 7RH, UK; mt350{at}le.ac.uk
Citation
Congenital monocular elevation deficiency associated with a novel TUBB3 gene variant
Publication history
- Received March 24, 2019
- Revised June 15, 2019
- Accepted June 23, 2019
- First published July 13, 2019.
Online issue publication
March 24, 2020
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© Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY. Published by BMJ. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/.