Progession of phenotype in Leber's congenital amaurosis with a mutation at the LCA5 locus
Author:
Publisher
BMJ
Subject
Cellular and Molecular Neuroscience,Sensory Systems,Ophthalmology
Cited by 31 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
1. Leber’s Congenital Amaurosis: Current Concepts of Genotype-Phenotype Correlations;Genes;2021-08-19
2. Voretigene Neparvovec and Gene Therapy for Leber’s Congenital Amaurosis: Review of Evidence to Date;The Application of Clinical Genetics;2020-11
Voretigene Neparvovec and Gene Therapy for Leber’s Congenital Amaurosis: Review of Evidence to Date
3. Treatment Potential for LCA5-Associated Leber Congenital Amaurosis;Investigative Opthalmology & Visual Science;2020-05-19
4. Retinitis Pigmentosa;Hereditary Chorioretinal Disorders;2020
5. Knocking out lca5 in zebrafish causes cone-rod dystrophy due to impaired outer segment protein trafficking;Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease;2019-10
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