Disorders of Sphingolipid Metabolism and Neuronal Ceroid-Lipofuscinoses

  • Vanier M
  • Caillaud C
N/ACitations
Citations of this article
1Readers
Mendeley users who have this article in their library.
Get full text

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...

Cite

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

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free