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Cell- and gene-based therapeutic approaches for neurological deficits in Mucopolysaccharidoses

Mucopolysaccharidoses (MPS) are a group of lysosomal storage diseases that are resulted from abnormal accumulation of glycosaminoglycans. Among the progressive multi-organ abnormalities often associated with MPS diseases, the deterioration of central nervous system (CNS) is the most challenging mani...

Täydet tiedot

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Bibliografiset tiedot
Päätekijä: Pan, Dao
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2011
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC4040261/
https://ncbi.nlm.nih.gov/pubmed/21235445
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