Type C Niemann-Pick disease. Lysosomal accumulation and defective intracellular mobilization of low density lipoprotein cholesterol.
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
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1. The Metabolic Basis of Inherited Disease;Brady,1983
2. THE CEREBRAL DEFECT IN TAY-SACHS DISEASE AND NIEMANN-PICK DISEASE
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
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