Familial lecithin-cholesterol acyltransferase deficiency: If so rare, why so frequent in the state of Piaui, northeastern Brazil?
de Serpa Brandão RMS, Britto FB, do Monte Neto JT, Lima MC, do Monte SJH, de Sousa Lima AV, Pereira EM, da Silva HJN, Oliveira DMTE, Coelho AGB, da Silva AS.
Mol Genet Metab Rep. 2022 Jan 3;30:100840. doi: 10.1016/j.ymgmr.2021.100840. eCollection 2022 Mar.
PMID:35242572
[Glomerulopathy associated with lecithin-cholesterol-acyltransferase deficiency: A case report and literature review].
Delteil C, Macagno N, Appay R, Uzan M, Jourde-Chiche N, Daniel L.
Ann Pathol. 2019 Apr;39(2):172-176. doi: 10.1016/j.annpat.2018.09.005. Epub 2018 Dec 12.
PMID:30553642
Familial lecithin:cholesterol acyltransferase deficiency: First-in-human treatment with enzyme replacement.