Type C Niemann-Pick disease. Abnormal metabolism of low density lipoprotein in homozygous and heterozygous fibroblasts.
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference19 articles.
1. The Metabolic Basis of Inherited Disease;Brady,1983
2. Proceedings of the International Symposium, Enzymes of Lipid Metabolism, Part II;Vanier,1986
3. The metabolism of sphingomyelin. II. Evidence of an enzymatic deficiency in Niemann-Pick diseae.
4. Sphingomyelinase in normal human spleens and in spleens from subjects with Niemann-Pick disease
5. A genetic storage disorder in BALB/C mice with a metabolic block in esterification of exogenous cholesterol.
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