Abstract
The sphingolipidoses are a group of inherited lysosomal storage diseases, which are caused by a defect in one or more sphingolipid degradation steps. The subsequent accumulation of nondegradable material in one or more organs leads to the expression of the disease....
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CITATION STYLE
APA
Hoops, S. L., Kolter, T., & Sandhoff, K. (2009). Sphingolipid-Inherited Diseases of the Central Nervous System. In Handbook of Neurochemistry and Molecular Neurobiology (pp. 671–702). Springer US. https://doi.org/10.1007/978-0-387-30378-9_27
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