Lack of evidence for reduced plasma apo B48 catabolism in patients with heterozygous familial hypercholesterolemia carrying the same null LDL receptor gene mutation.

Tremblay, André J

Lack of evidence for reduced plasma apo B48 catabolism in patients with heterozygous familial hypercholesterolemia carrying the same null LDL receptor gene mutation. [electronic resource] - Atherosclerosis Feb 2004 - 367-73 p. digital

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

0021-9150

10.1016/j.atherosclerosis.2003.11.011 doi


Adult
Apolipoprotein B-48
Apolipoproteins B--blood
Chylomicron Remnants
Chylomicrons--metabolism
Heterozygote
Humans
Hyperlipoproteinemia Type II--blood
Isotopes
Leucine
Male
Mutation
Receptors, LDL--genetics