Mutation Survey of Candidate Genes and Genotype–Phenotype Analysis in 20 Southeastern Chinese Patients with Axenfeld–Rieger Syndrome
Author:
Affiliation:
1. State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-Sen University, Guangzhou, China
Funder
National Natural Science Foundation of China
Publisher
Informa UK Limited
Subject
Cellular and Molecular Neuroscience,Sensory Systems,Ophthalmology
Link
https://www.tandfonline.com/doi/pdf/10.1080/02713683.2018.1493129
Reference33 articles.
1. Axenfeld–Rieger syndrome and spectrum of PITX2 and FOXC1 mutations
2. Genomics and anterior segment dysgenesis: a review
3. Erratum: Glaucoma spectrum and age-related prevalence of individuals with FOXC1 and PITX2 variants
4. Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome
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