A family of homozygous familial hyperalphalipoproteinemia with complete deficiency of cholesteryl ester transfer activity. [electronic resource]

By: Contributor(s): Producer: 19900731Description: 202-12 p. digitalISSN:
  • 0098-6127
Subject(s): In: Artery vol. 17
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

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