Published January 1, 1998
                      
                       | Version v1
                    
                    
                      
                        
                          Journal article
                        
                      
                      
                        
                          
                        
                        
                          Open
                        
                      
                    
                  Mutation of the Stargardt Disease Gene (ABCR) in Age-related Macular Degeneration:
Description
      Age-related macular degeneration (AMD) is the leading cause of severe central visual impairment among the elderly and is associated both with environmental factors such as smoking and with genetic factors. Here, 167 unrelated AMD patients were screened for alterations in ABCR, a gene that encodes a retinal rod photoreceptor protein and is defective in Stargardt disease, a common hereditary form of macular dystrophy. Thirteen different AMD-associated alterations, both deletions and amino acid substitutions, were found in one allele of ABCR in 26 patients (16%). Identification ofABCR alterations will permit presymptomatic testing of high-risk individuals and may lead to earlier diagnosis of AMD and to new strategies for prevention and therapy.
    
  Files
      
        article.pdf
        
      
    
    
      
        Files
         (571.0 kB)
        
      
    
    | Name | Size | Download all | 
|---|---|---|
| 
            
            md5:dfd0e16e6f89a97df43bbe92b5434e5b
             | 
          571.0 kB | Preview Download |