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- W171912801 endingPage "32" @default.
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- W171912801 abstract "The relationship of sphingolipids with human disease first arose from the study of sphingolipid storage diseases over 50 years ago. Most of these disorders are due to inherited deficiencies of specific sphingolipid hydrolases, although a small number also result from defects in sphingolipid transport or activator proteins. Due to the primary protein deficiencies sphingolipids and other macromolecules accumulate in cells and tissues of affected patients, leading to a diverse presentation of clinical abnormalities. Over 25 sphingolipid storage diseases have been described to date. Most of the genes have been isolated, disease-causing mutations have been identified, the recombinant proteins have been produced and characterized, and animal models exist for most of the human diseases. Since most sphingolipid hydrolases are enriched within the endosomal/lysosomal system, macromolecules first accumulate within these compartments. However, these abnormalities rapidly spread to other compartments and cause a wide range of cellular dysfunction. This review focuses on the genetics of sphingolipid storage diseases and related hydrolytic enzymes with an emphasis on the relationship between genetic mutations and human disease." @default.
- W171912801 created "2016-06-24" @default.
- W171912801 creator A5008143616 @default.
- W171912801 creator A5034341624 @default.
- W171912801 date "2013-01-01" @default.
- W171912801 modified "2023-09-27" @default.
- W171912801 title "The Genetics of Sphingolipid Hydrolases and Sphingolipid Storage Diseases" @default.
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