Abstract
Sphingolipidoses are a subgroup of lysosomal storage disorders in which sphingolipids accumulate in one or several organs as the result of a primary deficiency in enzymes or activator proteins involved in their degradative pathway. Traditionally, this subgroup also...
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CITATION STYLE
APA
Vanier, M. T., & Caillaud, C. (2012). Disorders of Sphingolipid Metabolism and Neuronal Ceroid-Lipofuscinoses. In Inborn Metabolic Diseases (pp. 555–577). Springer Berlin Heidelberg. https://doi.org/10.1007/978-3-642-15720-2_39
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