Llwytho...

Small-molecule therapeutics for the treatment of glycolipid lysosomal storage disorders.

Glycosphingolipid (GSL) lysosomal storage disorders are a small but challenging group of human diseases to treat. Although these disorders appear to be monogenic in origin, where the catalytic activity of enzymes in GSL catabolism is impaired, the clinical presentation and severity of disease are he...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Butters, Terry D, Mellor, Howard R, Narita, Keishi, Dwek, Raymond A, Platt, Frances M
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: 2003
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC1693180/
https://ncbi.nlm.nih.gov/pubmed/12803927
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1098/rstb.2003.1278
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