The two novel CETP mutations Gln87X and Gln165X in a compound heterozygous state are associated with marked hyperalphalipoproteinemia and absence of significant coronary artery disease

2006 ◽  
Vol 84 (8) ◽  
pp. 647-650 ◽  
Author(s):  
Jeffrey Rhyne ◽  
Michael J. Ryan ◽  
Charles White ◽  
Theodore Chimonas ◽  
Michael Miller
2015 ◽  
Vol 16 (9) ◽  
pp. 1015-1022 ◽  
Author(s):  
Ivan Stankovic ◽  
Biljana Putnikovic ◽  
Aleksandra Janicijevic ◽  
Milica Jankovic ◽  
Radosava Cvjetan ◽  
...  

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