Novel homozygous splicing mutations in ARL2BP cause autosomal recessive retinitis pigmentosa

Fiorentino, A, Yu, J, Arno, G et al. (28 more authors) (2018) Novel homozygous splicing mutations in ARL2BP cause autosomal recessive retinitis pigmentosa. Molecular Vision, 24. pp. 603-612. ISSN 1090-0535

Abstract

Metadata

Authors/Creators:
Dates:
  • Published: 31 August 2018
  • Accepted: 29 August 2018
Institution: The University of Leeds
Academic Units: The University of Leeds > Faculty of Medicine and Health (Leeds) > School of Medicine (Leeds) > Inst of Biomed & Clin Sciences (LIBACS) (Leeds) > Genetics (LIBACS) (Leeds)
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: 15 Oct 2018 10:27
Last Modified: 15 Oct 2018 10:29
Status: Published
Publisher: http://www.molvis.org/molvis/toc.html

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