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

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 Spectral-Domain Optical Coherence Tomography (SD-OCT) and correl...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Front Neuroanat
Egile Nagusiak: Cuenca, Nicolás, Fernández-Sánchez, Laura, Sauvé, Yves, Segura, Francisco J., Martínez-Navarrete, Gema, Tamarit, José Manuel, Fuentes-Broto, Lorena, Sanchez-Cano, Ana, Pinilla, Isabel
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Frontiers Media S.A. 2014
Gaiak:
Neuroscience
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC4273614/
https://ncbi.nlm.nih.gov/pubmed/25565976
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fnana.2014.00151
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