Advances in the genetics of eye diseases
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Pediatrics, Perinatology and Child Health
Reference27 articles.
1. Mutations in TMEM231 cause Joubert syndrome in French Canadians.;Srour;J Med Genet,2012
2. Mutations in C5ORF42 cause Joubert syndrome in the French Canadian population.;Srour;Am J Hum Genet,2012
3. USH1K, a novel locus for type I Usher syndrome, maps to chromosome 10p11.21-q21.1.;Jaworek;J Hum Genet,2012
4. A direct and melanopsin-dependent fetal light response regulates mouse eye development.;Rao;Nature,2013
5. Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia.;Verhoeven;Nat Genet,2013
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3. CRISPR/Cas9 genome surgery for retinal diseases;Drug Discovery Today: Technologies;2018-08
4. VSX1 and SOD1 mutation screening in patients with keratoconus;Journal of Ophthalmic and Vision Research;2018
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