✦ LIBER ✦
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
✍ Scribed by Jeffrey Rhyne; Michael J. Ryan; Charles White; Theodore Chimonas; Michael Miller
- Book ID
- 105796440
- Publisher
- Springer
- Year
- 2006
- Tongue
- English
- Weight
- 136 KB
- Volume
- 84
- Category
- Article
- ISSN
- 0946-2716
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