Associated Papers
A systematic review of the natural history and biomarkers of primary lecithin:cholesterol acyltransferase deficiency.
Vitali C et al.
Journal of Lipid Research, 2022
35065092 (PubMed )
Supplement: mmc1.pdf
LCAT deficiency: a systematic review with the clinical and genetic description of Mexican kindred.
Mehta R et al.
Lipids in Health and Disease, 2021
Finding a very rare mutation in non-Caucasian LCAT patients from Southwest Asia for the first time.
Oliaei F et al.
Journal of Cellular Biochemistry, 2019
Marked HDL deficiency and premature coronary heart disease.
Schaefer EJ et al.
Current Opinion in Lipidology, 2010
Characterization of a new LCAT mutation causing familial LCAT deficiency (FLD) and the role of APOE as a modifier gene of the FLD phenotype.
Baass A et al.
Atherosclerosis, 2009
Select a paper to view details