Correlation between SD-OCT, immunocytochemistry and functional findings in an animal model of retinal degeneration

Volume: 8, Pages: 151 - 151
Published: Dec 22, 2014
Abstract
Purpose: The P23H rhodopsin mutation is an autosomal dominant cause of retinitis pigmentosa (RP). The degeneration can be tracked using different anatomical and functional methods. In our case, we evaluated the anatomical changes using SpectralDomain Optical Coherence Tomography (SD-OCT) and correlated the findings with retinal thickness values determined by immunocytochemistry. Methods: Pigmented rats heterozygous for the P23H mutation, with...
Paper Details
Title
Correlation between SD-OCT, immunocytochemistry and functional findings in an animal model of retinal degeneration
Published Date
Dec 22, 2014
Volume
8
Pages
151 - 151
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