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LCAT gene

Discuss publications and research concerning the LCAT gene.

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Related literature

Novel pathogenic variant in the LCAT gene in a compound heterozygous patient with fish-eye disease and a mild phenotype.
LCAT
Rescue of Familial Lecithin:Cholesterol Acyltranferase Deficiency Mutations with an Allosteric Activator.
LCAT
A thumbwheel mechanism for APOA1 activation of LCAT activity in HDL.
LCAT
Novel metabolic phenotypes in lecithin cholesterol acyltyransferase-deficient mice.
LCAT
CETP and LCAT Gene Polymorphisms Are Associated with High-Density Lipoprotein Subclasses and Acute Coronary Syndrome.
LCAT
Plasma levels of Apolipoprotein A1 and Lecithin:Cholesterol Acyltransferase in type 2 diabetes mellitus: Correlations with haptoglobin phenotypes.
LCAT
The high-resolution crystal structure of human LCAT.
LCAT
Premature and severe cardiovascular disease in a Mexican male with markedly low high-density-lipoprotein-cholesterol levels and a mutation in the lecithin:cholesterol acyltransferase gene: a family study.
LCAT
Adrenal Function in females with low plasma HDL-C due to mutations in ABCA1 and LCAT.
LCAT
Lecithin-cholesterol acyltransferase (LCAT) deficiency without mutations in the coding sequence: a case report and literature review.
LCAT

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