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Therapeutic approaches for lysosomal storage diseases

The lysosomal storage disorders (LSDs) comprise a heterogeneous group of inborn errors of metabolism characterized by tissue substrate deposits, most often caused by a deficiency of the enzyme normally responsible for catabolism of various byproducts of cellular turnover. Individual entities are typ...

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Kaydedildi:
Detaylı Bibliyografya
Yazar: Pastores, Gregory M.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: SAGE Publications 2010
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3474616/
https://ncbi.nlm.nih.gov/pubmed/23148162
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/2042018810384429
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