Congenital hereditary endothelial dystrophy caused by SLC4A11 mutations progresses to Harboyan syndrome.

Siddiqui, S, Zenteno, JC, Rice, A et al. (8 more authors) (2014) Congenital hereditary endothelial dystrophy caused by SLC4A11 mutations progresses to Harboyan syndrome. Cornea, 33 (3). 247 - 251. ISSN 0277-3740

Abstract

Metadata

Authors/Creators:
  • Siddiqui, S
  • Zenteno, JC
  • Rice, A
  • Chacón-Camacho, O
  • Naylor, SG
  • Rivera-de la Parra, D
  • Spokes, DM
  • James, N
  • Toomes, C
  • Inglehearn, CF
  • Ali, M
Copyright, Publisher and Additional Information: © 2013 by Lippincott Williams & Wilkins. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Keywords: corneal endothelial dystrophy, Harboyan syndrome, sensorineural hearing loss, SLC4A11
Dates:
  • Published: March 2014
Institution: The University of Leeds
Academic Units: The University of Leeds > Faculty of Medicine and Health (Leeds) > Institute of Molecular Medicine (LIMM) (Leeds) > Section of Opthalmology and Neurosciences (Leeds)
Depositing User: Symplectic Publications
Date Deposited: 28 Oct 2015 16:57
Last Modified: 29 Oct 2015 09:50
Published Version: http://dx.doi.org/10.1097/ICO.0000000000000041
Status: Published
Publisher: Lippincott, Williams & Wilkins
Identification Number: https://doi.org/10.1097/ICO.0000000000000041
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