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Diagnosis of human peroxisomal disorders: A handbook Roels Reprinted from the Journal of Inherited Metabolic edition
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Diagnosis of human peroxisomal disorders: A handbook
Roels
These include microscopic studies, analysis of metabolites (very long-chain fatty acids, bile acids, and plasmalogens), enzyme studies (peroxisomal beta-oxidation pathway and dihydroxyacetone phosphate acyltransferase), immunodetection of peroxisomal (membrane) proteins and molecular analysis of mutant DNA.
232 pages, index
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