(Q53528346)
Statements
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. (English)
Jeffrey Rhyne
Michael J Ryan
Charles White
Theodore Chimonas
Michael Miller
20 July 2006
84
8
647-650
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