Achromatopsie congénitale : intérêt de l’électrorétinogramme pour le diagnostic précoce
Author:
Publisher
Elsevier BV
Subject
Ophthalmology
Reference22 articles.
1. Krill AE. The electroretinogram in congenital colour vision defects. The clinical value of electroretinography 1968, ISCERG Symp. et Ghent 1966, 205-14.
2. The photoreceptors in the achromat;Sharpe,1990
3. L’achromatopsie congénitale;François;Doc Ophthalmol,1995
4. Rod and Cone receptor mechanisms in typical and atypical congenital achromatopsia;Blackwell;Vision Res,1961
5. Total colour-blindness: an introduction;Sharpe,1990
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1. Contribution du SD-OCT de la macula dans le diagnostic de l’achromatopsie congénitale : à propos de 6 patients;Journal Français d'Ophtalmologie;2014-04
2. CNGA3 Deficiency Affects Cone Synaptic Terminal Structure and Function and Leads to Secondary Rod Dysfunction and Degeneration;Investigative Opthalmology & Visual Science;2012-03-01
3. Clinical and genetic investigation of a large Tunisian family with complete achromatopsia: identification of a new nonsense mutation in GNAT2 gene;Journal of Human Genetics;2010-11-25
4. Generalized Inherited Retinal Dystrophies;Pediatric Retina;2010-08-19
5. Rod and Rod-Driven Function in Achromatopsia and Blue Cone Monochromatism;Investigative Opthalmology & Visual Science;2009-02-01
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