martes, 25 de febrero de 2020

Persistent dyslipidemia in treatment of lysosomal acid lipase deficiency | Orphanet Journal of Rare Diseases | Full Text

Persistent dyslipidemia in treatment of lysosomal acid lipase deficiency | Orphanet Journal of Rare Diseases | Full Text

Lysosomal acid lipase deficiency (LALD) is an autosomal recessive inborn error of lipid metabolism characterized by impaired lysosomal hydrolysis and consequent accumulation of cholesteryl esters and triglycer...
Authors:Amanda Barone Pritchard, Alanna Strong and Can Ficicioglu
Citation:Orphanet Journal of Rare Diseases 2020 15:58
Content type:Research
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