Imino sugar inhibitors for treating the lysosomal glycosphingolipidoses.

The inherited metabolic disorders of glycosphingolipid (GSL) metabolism are a relatively rare group of diseases that have diverse and often neurodegenerative phenotypes. Typically, a deficiency in catabolic enzyme activity leads to lysosomal storage of GSL substrates and in many diseases, several ot...

詳細記述

書誌詳細
主要な著者: Butters, T, Dwek, R, Platt, F
フォーマット: Journal article
言語:English
出版事項: 2005