Leber congenital amaurosis: Genes, proteins and disease mechanisms
Author:
Publisher
Elsevier BV
Subject
Sensory Systems,Ophthalmology
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1. Clinical, Ophthalmic, and Genetic Characterization of RPGRIP1-Associated Leber Congenital Amaurosis/Early-Onset Severe Retinal Dystrophy;American Journal of Ophthalmology;2024-10
2. Clinical and Molecular Characterization of AIPL1-Associated Leber Congenital Amaurosis/Early-Onset Severe Retinal Dystrophy;American Journal of Ophthalmology;2024-10
3. Perturbed cell cycle phase-dependent positioning and nuclear migration of retinal progenitors along the apico-basal axis underlie global retinal disorganization in the LCA8-like mouse model;Developmental Biology;2024-09
4. Publication trends of Leber congenital amaurosis researches: a bibliometric study during 2002-2022;International Journal of Ophthalmology;2024-08-18
5. Cross-species single-cell landscapes identify the pathogenic gene characteristics of inherited retinal diseases;Frontiers in Genetics;2024-07-11
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