A family of homozygous familial hyperalphalipoproteinemia with complete deficiency of cholesteryl ester transfer activity.

Eto, M

A family of homozygous familial hyperalphalipoproteinemia with complete deficiency of cholesteryl ester transfer activity. [electronic resource] - Artery 1990 - 202-12 p. digital

Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

0098-6127


Adolescent
Adult
Apolipoproteins--blood
Carboxylic Ester Hydrolases--deficiency
Child
Child, Preschool
Cholesterol, HDL--blood
Female
Homozygote
Humans
Hyperlipoproteinemia Type II--genetics
Isoelectric Focusing
Male
Pedigree
Sterol Esterase--deficiency
Ultracentrifugation