Frohlich_1982_Am.J.Hum.Genet_34_65

Reference

Title : Detection of heterozygotes for familial lecithin: cholesterol acyltransferase (LCAT) deficiency - Frohlich_1982_Am.J.Hum.Genet_34_65
Author(s) : Frohlich J , Hon K , McLeod R
Ref : American Journal of Human Genetics , 34 :65 , 1982
Abstract :

"Rocket" immunoelectrophoresis using specific anti-lecithin: cholesterol acyltransferase (LCAT) antiserum showed no immunoreactive protein in two patients with familial LCAT deficiency. Subnormal quantity of plasma LCAT was found in the maternal grandmother, the parents, and in two of four siblings of the patients (3.3-3.4 mg/l vs. 5.4 +/- 0.5 mg/l in 12 controls). The immunochemical quantitation of the enzyme correlated well (r = .93) with LCAT activity in an artificial substrate assay. These two methods allow detection of heterozygotes for LCAT deficiency.

PubMedSearch : Frohlich_1982_Am.J.Hum.Genet_34_65
PubMedID: 6805319

Citations formats

Frohlich J, Hon K, McLeod R (1982)
Detection of heterozygotes for familial lecithin: cholesterol acyltransferase (LCAT) deficiency
American Journal of Human Genetics 34 :65

Frohlich J, Hon K, McLeod R (1982)
American Journal of Human Genetics 34 :65