Molecular genetics with clinical characteristics of Leber congenital amaurosis in the Han population of western China
Author:
Affiliation:
1. Southwest Hospital/Southwest Eye Hospital, Army Medical University, Chongqing, China
2. Key Lab of Visual Damage and Regeneration & Restoration of Chongqing, Army Medical University, Chongqing, China
Funder
The National Key R&D Program of China
The Foundation of Southwest Hospital
Publisher
Informa UK Limited
Subject
Genetics (clinical),Ophthalmology,Pediatrics, Perinatology and Child Health
Link
https://www.tandfonline.com/doi/pdf/10.1080/13816810.2021.1904417
Reference34 articles.
1. Correction: Leber congenital amaurosis/early-onset severe retinal dystrophy: clinical features, molecular genetics and therapeutic interventions
2. Leber congenital amaurosis/early-onset severe retinal dystrophy: clinical features, molecular genetics and therapeutic interventions
3. Review and update on the molecular basis of Leber congenital amaurosis
4. Leber congenital amaurosis: Genes, proteins and disease mechanisms
5. Unravelling the Complexity of Inherited Retinal Dystrophies Molecular Testing: Added Value of Targeted Next-Generation Sequencing
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