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)
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pp. 647-650
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2008 ◽
Vol 2
(1)
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pp. 14-16
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2019 ◽
Vol 293
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pp. 278-285
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2015 ◽
Vol 16
(9)
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pp. 1015-1022
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2007 ◽
Vol 50
(15)
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pp. 1469-1475
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2006 ◽
Vol 48
(8)
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pp. 1579-1587
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