LC-MS/MS-based enzyme assay for lysosomal acid lipase using dried blood spots

Lysosomal acid lipase deficiency (LAL-D) (OMIM: 278000) is a lysosomal storage disorder with two distinct disease phenotypes such as Wolman disease and cholesteryl ester storage disorder (CESD), characterized by an accumulation of endocytosed cholesterol in the body. Due to the presence of multiple...

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Bibliographic Details
Main Authors: Mari Ohira, Marianne Barr, Torayuki Okuyama, Ryuichi Mashima
Format: Article
Language:English
Published: Elsevier 2022-12-01
Series:Molecular Genetics and Metabolism Reports
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2214426922000738