Oligocone trichromacy is part of the spectrum ofCNGA3-related cone system disorders
Author:
Publisher
Informa UK Limited
Subject
Genetics (clinical),Ophthalmology,Pediatrics, Perinatology and Child Health
Link
http://www.tandfonline.com/doi/pdf/10.3109/13816810.2010.544366
Reference18 articles.
1. General Cone Dysfunction without Achromatopsia
2. Foveal densitometry and color matching in oligocone trichromacy
3. Variant Phenotypes of Incomplete Achromatopsia in Two Cousins withGNAT2Gene Mutations
4. Oligocone Trichromacy: Clinical and Molecular Genetic Investigations
5. Mutations in CNGA3 impair trafficking or function of cone cyclic nucleotide-gated channels, resulting in achromatopsia
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3. Molecular and clinical characterization of Thai patients with achromatopsia: identification of three novel disease-associated variants in the CNGA3 and CNGB3 genes;International Ophthalmology;2020-08-31
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