Leber congenital amaurosis: Clinical correlations with genotypes, gene therapy trials update, and future directions
Author:
Publisher
Elsevier BV
Subject
Ophthalmology,Pediatrics, Perinatology and Child Health
Reference41 articles.
1. Crumbs homolog1 (CRB1) mutations result in a thick human retina with abnormal lamination;Jacobson;Hum Mol Gen,2003
2. Genetic testing for retinal dystrophies and dysfunctions: Benefits, dilemmas and solutions;Koenekoop;Clin Exp Ophthalmol,2007
3. Leber congenital amaurosis—A model for efficient genetic testing of heterogeneous disorders: LXIV Edward Jackson Memorial Lecture;Stone;Am J Ophthalmol,2007
4. An overview of Leber Congenital Amaurosis: A model to understand human development;Koenekoop;Surv Ophthalmol,2004
5. Genetic isolates in ophthalmic diseases;Sherwin;Ophthalm Genet,2008
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