Plasma FA composition in familial LCAT deficiency indicates SOAT2-derived cholesteryl ester formation in humans

Abstract: Mutations in the LCAT gene cause familial LCAT deficiency (Online Mendelian Inheritance in Man ID: #245900), a very rare metabolic disorder. LCAT is the only enzyme able to esterify cholesterol in plasma, whereas sterol O-acyltransferases 1 and 2 are the enzymes esterifying cellular choles...

ver descrição completa

Detalhes bibliográficos

Principais autores:	Chiara Pavanello, Alice Ossoli, Arianna Strazzella, Patrizia Risè, Fabrizio Veglia, Marie Lhomme, Paolo Parini, Laura Calabresi
Formato:	Artigo
Idioma:	Inglês
Publicado em:	Elsevier 2022-07-01
coleção:	Journal of Lipid Research
Assuntos:	familial LCAT deficiency cholesteryl esters lipoproteins SOAT2 cholesteryl ester FAs VLDL
Acesso em linha:	http://www.sciencedirect.com/science/article/pii/S0022227522000657
Tags:	Adicionar Tag Sem tags, seja o primeiro a adicionar uma tag!