Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Ophthalmology,General Medicine
Reference28 articles.
1. Special issue introduction: inherited retinal disease: novel candidate genes, genotype-phenotype correlations, and inheritance models;Cremers;Genes (Basel),2018
2. Homozygosity for a novel double mutant allele (G1961E/L857P) underlies childhood-onset ABCA4-related retinopathy in the United Arab Emirates;Khan;Retina,2019
3. Microcornea with myopic chorioretinal atrophy, telecanthus and posteriorly-rotated ears: a distinct clinical syndrome;Khan;Ophthalmic Genet,2012
4. The syndrome of microcornea, myopic chorioretinal atrophy, and telecanthus (MMCAT) is caused by mutations in ADAMTS18;Aldahmesh;Hum Mutat,2013
5. Ophthalmic features of children not yet diagnosed with Alstrom syndrome;Khan;Ophthalmology,2015
Cited by
24 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献