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Pathomechanisms in Lysosomal Storage Disorders

Lysosomal diseases are inherited metabolic disorders caused by defects in a wide spectrum of lysosomal and a few non-lysosomal proteins. In most cases a single type of primary storage material is identified, which has been used to name and classify the disorders: hence the terms sphingolipidoses, ga...

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Detalhes bibliográficos
Publicado no:Biochim Biophys Acta
Main Authors: Walkley, Steven U., Vanier, Marie T.
Formato: Artigo
Idioma:Inglês
Publicado em: 2008
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4382014/
https://ncbi.nlm.nih.gov/pubmed/19111580
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bbamcr.2008.11.014
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