Identification of a novel splice-site mutation in the Lebercilin (LCA5) gene causing Leber congenital amaurosis

Ramprasad, VL, Soumittra, N, Nancarrow, D et al. (7 more authors) (2008) Identification of a novel splice-site mutation in the Lebercilin (LCA5) gene causing Leber congenital amaurosis. Molecular Vision, 10 (14). pp. 481-486. ISSN 1090-0535

Abstract

Metadata

Authors/Creators:
  • Ramprasad, VL
  • Soumittra, N
  • Nancarrow, D
  • Sen, P
  • McKibbin, M
  • Williams, GA
  • Arokiasamy, T
  • Lakshmipathy, P
  • Inglehearn, CF
  • Kumaramanickavel, G
Keywords: Leber congenital amaurosis; Lebercillin; (LCA5)
Dates:
  • Published: 10 March 2008
  • Accepted: 5 February 2008
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: 05 Sep 2019 10:47
Last Modified: 05 Sep 2019 10:47
Published Version: http://www.molvis.org/molvis/v14/a57/
Status: Published
Publisher: Molecular Vision

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