Progression of chronic kidney disease in familial LCAT deficiency: a follow-up of the Italian cohort.
Sign Up to like & getrecommendations! Published in 2020 at "Journal of lipid research"
DOI: 10.1194/jlr.p120000976
Abstract: Familial LCAT deficiency (FLD) is a rare genetic disorder of HDL metabolism, caused by loss-of-function mutations in the LCAT gene and characterized by a variety of symptoms including corneal opacities and kidney failure. Renal disease… read more here.
Keywords: familial lcat; deficiency; disease; kidney ... See more keywords