Co-Authors
                            
                            
                                This is a "connection" page, showing publications co-authored by   LINDSAY BURRAGE   and   I-WEN SONG.
                            
                            
                            
                                
                                    
                                            
    
        
        
        
            Connection Strength
            
                
            
            0.136
         
        
        
     
 
    
        
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            Dominant negative variants in KIF5B cause osteogenesis imperfecta via down regulation of mTOR signaling. PLoS Genet. 2023 Nov; 19(11):e1011005.
            
            
                Score: 0.054
            
         
        
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            COPB2 loss of function causes a coatopathy with osteoporosis and developmental delay. Am J Hum Genet. 2021 09 02; 108(9):1710-1724.
            
            
                Score: 0.047
            
         
        
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            Heterozygous variants in ACTL6A, encoding a component of the BAF complex, are associated with intellectual disability. Hum Mutat. 2017 10; 38(10):1365-1371.
            
            
                Score: 0.035