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.

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🔗 View Article (PMID 16855848)

Published in J Mol Med (Berl) on July 20, 2006

Authors

Jeffrey Rhyne1, Michael J Ryan, Charles White, Theodore Chimonas, Michael Miller

Author Affiliations

1: University of Maryland and Veterans Affairs Medical Center, Baltimore, MD, USA.

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