Eto, M <br/><br/>
A family of homozygous familial hyperalphalipoproteinemia with complete deficiency of cholesteryl ester transfer activity.  [electronic resource] 

 -  Artery  1990 
 - 202-12 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0098-6127 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Apolipoproteins--blood<br/>Carboxylic Ester Hydrolases--deficiency<br/>Child<br/>Child, Preschool<br/>Cholesterol, HDL--blood<br/>Female<br/>Homozygote<br/>Humans<br/>Hyperlipoproteinemia Type II--genetics<br/>Isoelectric Focusing<br/>Male<br/>Pedigree<br/>Sterol Esterase--deficiency<br/>Ultracentrifugation