Associated Papers
Black Patients Equally Benefit From Renal Genetics Evaluation but Substantial Barriers in Access Exist.
Borden C et al.
Kidney International Reports, 2023
37850009 (PubMed )
Supplement: mmc1.pdf
A novel pathogenic variant in LCAT causing FLD. A case report.
Goñi Ros N et al.
Acta Clinica Belgica, 2022
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
Analysis of rare genetic variation underlying cardiometabolic diseases and traits among 200,000 individuals in the UK Biobank.
Jurgens SJ et al.
Nature Genetics, 2022
LCAT deficiency: a systematic review with the clinical and genetic description of Mexican kindred.
Mehta R et al.
Lipids in Health and Disease, 2021
Genome-wide rare variant analysis for thousands of phenotypes in over 70,000 exomes from two cohorts.
Cirulli ET et al.
Nature Communications, 2020
31992710 (PubMed )
Supplement: 41467_2020_14288_MOESM1_ESM.pdf
Very low levels of HDL cholesterol and atherosclerosis, a variable relationship--a review of LCAT deficiency.
Savel J et al.
Vascular Health and Risk Management, 2012
Characterization of antioxidant/anti-inflammatory properties and apoA-I-containing subpopulations of HDL from family subjects with monogenic low HDL disorders.
Daniil G et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry, 2011
Paradoxical fall in proteinuria during pregnancy in an LCAT-deficient patient-A case report.
Hanna EV et al.
Journal of Clinical Lipidology, 0
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