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

Author： Rhyne Jeffrey   Ryan Michael   White Charles   Chimonas Theodore   Miller Michael  

Publisher： Springer Publishing Company

ISSN： 0946-2716

Source： Journal of Molecular Medicine, Vol.84, Iss.8, 2006-08, pp. : 647-650

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