Advanced Imaging and Cytometric Techniques to Characterize Lipid Accumulation in Wolman Disease
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DOI: 10.1002/cyto.a.24949
Abstract: Wolman disease (WD) is a severe lysosomal storage disorder characterized by fatal lipid accumulation caused by the deficiency of a lipid metabolic enzyme, Lysosomal Acid Lipase (LAL), involved in the lysosomal hydrolysis of cholesterols and… read more here.
Keywords: lal deficient; wolman disease; lipid accumulation;