Substrate reduction therapy

The glycosphingolipidoses are a family of storage diseases that arise due to incomplete catabolism of glycosphingolipids (GSLs) in the lysosome (Wraith, 2002). The majority are autosomal recessive disorders and result from mutations in the genes that encode the catabolic enzymes of the lysosome (Win...

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Dades bibliogràfiques
Autors principals: Platt, F, Butters, T
Format: Book section
Publicat: Springer US 2007

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