Ophthalmic manifestations of Heimler syndrome due to PEX6 mutations

Wangtiraumnuay, N, Alnabi, WA, Tsukikawa, M et al. (5 more authors) (2018) Ophthalmic manifestations of Heimler syndrome due to PEX6 mutations. Ophthalmic Genetics, 39 (3). pp. 384-390. ISSN 1381-6810

Abstract

Metadata

Authors/Creators:
Keywords: Heimler syndrome, macular dystrophy, PEX6
Dates:
  • Published: 4 May 2018
  • Accepted: 21 January 2018
  • Published (online): 20 April 2018
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)
Funding Information:
FunderGrant number
Fight for SightGR586
Depositing User: Symplectic Publications
Date Deposited: 02 May 2018 08:54
Last Modified: 04 May 2018 09:37
Status: Published
Publisher: Taylor & Francis
Identification Number: https://doi.org/10.1080/13816810.2018.1432063

Download not available

A full text copy of this item is not currently available from White Rose Research Online

Share / Export

Statistics