Structural bases of Wolman disease and cholesteryl ester storage disease
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism
Reference20 articles.
1. Acid lipase deficiency: Wolman disease and cholesteryl ester storage disease;Assmann,2001
2. Genetic and biochemical evidence that CESD and Wolman disease are distinguished by residual lysosomal acid lipase activity;Aslanidis;Genomics,1996
3. Mutations at the lysosomal acid cholesteryl ester hydrolase gene locus in Wolman disease;Anderson;Proc. Natl. Acad. Sci. U. S. A.,1994
4. Expression of lysosomal acid lipase mutants detected in three patients with cholesteryl ester storage disease;Pagani;Hum. Mol. Genet.,1996
5. Characterization of lysosomal acid lipase by site-directed mutagenesis and heterologous expression;Sheriff;J. Biol. Chem.,1995
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