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

Purpose: The P23H rhodopsin mutation is an autosomal dominant cause of retinitis pigmentosa. The degeneration can be tracked using different anatomical and functional methods. In our case, we evaluated the anatomical changes using Spectral-Domain Optical Coherence Tomography (SD-OCT) and correlated...

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Detalhes bibliográficos

Principais autores:	Nicolás eCuenca, Laura eFernandez-Sanchez, Yves eSauvé, Francisco Javier Segura, Gema Concepcion Martínez-Navarrete, Jose Manuel Tamarit, Lorena eFuentes-Broto, Ana eSanchez-Cano, Isabel ePinilla
Formato:	Artigo
Idioma:	Inglês
Publicado em:	Frontiers Media S.A. 2014-12-01
coleção:	Frontiers in Neuroanatomy
Assuntos:	Immunohistochemistry Retinal Degeneration Retinitis Pigmentosa Visual Acuity Electroretinogram Optical Coherence Tomography
Acesso em linha:	http://journal.frontiersin.org/Journal/10.3389/fnana.2014.00151/full
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