FIGURE
            Figure S1
- ID
 - ZDB-FIG-190812-6
 - Publication
 - Ouyang et al., 2019 - CPSF1 mutations are associated with early-onset high myopia and involved in retinal ganglion cell axon projection
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                        Figure S1
                    
                    
                
                
            
        
        
    
        
            
            
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 . Available fundus changes of the probands HM693 and HM949 and ERG recording of the proband HM693. (A) Typical fundus changes of high myopia, including an optic nerve head crescent and a “tigroid” appearance of the posterior retina. (B) ERG recording of the proband HM693 showed severely reduced cone responses and mildly reduced rod responses  | 
    
                
                    
                        Expression Data
                    
                    
                
                
            
        
        
    
        
            
            
            
            
    
    
                
                    
                        Expression Detail
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Antibody Labeling
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Phenotype Data
                    
                    
                
                
            
        
        
    
        
            
            
            
            
    
    
                
                    
                        Phenotype Detail
                    
                    
                
                
            
        
        
    
        
            
                
            
        
    
    
    
                
                    
                        Acknowledgments
                    
                    
                
                
            
        
        
    
        
            
            
                
                    
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      Full text @ Hum. Mol. Genet.