Detection of single nucleotide polymorphism of all coding region in ABCA1 gene and relationship among R1587K and plasma lipids and coronary artery disease
	    		
		   		
	    	
    	
    	
   		
        
        	
        		- VernacularTitle:ABCA1基因编码区SNP检测及R1587K与血脂和冠心病的关系
 
        	
        	
        	
        		- Author:
	        		
		        		
		        		
			        		Yayang LIU
			        		
			        		;
		        		
		        		
		        		
			        		Zhigang GUO
			        		
			        		;
		        		
		        		
		        		
			        		Yan TU
			        		
			        		
		        		
		        		
		        		
		        		
		        		
			        		
			        		
		        		
	        		
        		 
        	
        	
        	
        		- Publication Type:Journal Article
 
        	
        	
        		- Keywords:
        			
	        			
	        				
	        				
			        		
				        		ATP binding cassette transporter A1;
			        		
			        		
			        		
				        		polymorphism, single nucleotide;
			        		
			        		
			        		
				        		genes, ABCA1;
			        		
			        		
			        		
				        		coronary disease;
			        		
			        		
			        		
				        		hyperlipidemia
			        		
			        		
	        			
        			
        		
 
        	
            
            
            	- From:
	            		
	            			Medical Journal of Chinese People's Liberation Army
	            		
	            		 1981;0(04):-
	            	
            	
 
            
            
            	- CountryChina
 
            
            
            	- Language:Chinese
 
            
            
            	- 
		        	Abstract:
			       	
			       		
				        
				        	0.05). Conclusion The genotypes of ABCA1 R1587K polymorphism were associated closely with the plasma levels of HDL-C. The HDL-C levels of K allele carriers were remarkably lower. However, there was no significant association of the ABCA1 R1587K polymorphism and the susceptibility to CAD.