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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
Jeffrey Rhyne, Michael J. Ryan, Charles White, Theodore Chimonas, Michael MillerVolume:
84
Language:
english
Pages:
4
DOI:
10.1007/s00109-006-0070-4
Date:
August, 2006
File:
PDF, 136 KB
english, 2006