The P274S Mutation of Lecithin-Cholesterol Acyltransferase (LCAT) and Its Clinical Manifestations in a Large Kindred

Author:

Fountoulakis Nikolaos,Lioudaki Eirini,Lygerou Dimitra,Dermitzaki Eleftheria-Kleio,Papakitsou Ioanna,Kounali Vasiliki,Holleboom Adriaan G.,Stratigis Spyros,Belogianni Christina,Syngelaki Paraskevi,Stratakis Stavros,Evangeliou Athanasios,Gakiopoulou Hariklia,Kuivenhoven Jan Albert,Wevers Ron,Dafnis Eugene,Stylianou Kostas

Publisher

Elsevier BV

Subject

Nephrology

Reference47 articles.

1. Plasma lipoproteins in familial lecithin: cholesterol acyltransferase deficiency: structure of low and high density lipoproteins as revealed by elctron microscopy;Forte;J Clin Invest,1971

2. A review on lecithin:cholesterol acyltransferase deficiency;Saeedi;Clin Biochem,2015

3. The molecular pathology of lecithin:cholesterol acyltransferase (LCAT) deficiency syndromes;Kuivenhoven;J Lipid Res,1997

4. Atherogenic impact of lecithin-cholesterol acyltransferase and its relation to cholesterol esterification rate in HDL (FER(HDL)) and AIP [log(TG/HDL-C)] biomarkers: the butterfly effect?;Dobiášová;Physiol Res,2017

5. A study of the small spherical high density lipoproteins of patients afflicted with familial lecithin: cholesterol acyltransferase deficiency;Chen;J Lipid Res,1984

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