Congenital macular scars in siblings from CLDN19 mutations
Author:
Publisher
Elsevier BV
Subject
Ophthalmology,Pediatrics, Perinatology, and Child Health
Reference9 articles.
1. Structural grading of foveal hypoplasia using spectral-domain optical coherence tomography a predictor of visual acuity?;Thomas;Ophthalmology,2011
2. Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis: clinical and molecular characteristics;Claverie-Martin;Clin Kidney J,2015
3. Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: phenotype-genotype correlation and outcome in 32 patients with CLDN16 or CLDN19 mutations;Godron;Clin J Am Soc Nephrol,2012
4. Renal, ocular, and neuromuscular involvements in patients with CLDN19 mutations;Faguer;Clin J Am Soc Nephrol,2011
5. Familial non-syndromic macular pseudocoloboma secondary to homozygous CLDN19 mutation;Khan;Ophthalmic Genet,2018
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