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Central Nervous System Pathology Progresses Independently of KC and CXCR2 in Globoid-Cell Leukodystrophy

Globoid-cell Leukodystrophy (GLD; Krabbe’s disease) is a rapidly progressing inherited demyelinating disease caused by a deficiency of the lysosomal enzyme Galactosylceramidase (GALC). Deficiency of GALC leads to altered catabolism of galactosylceramide and the cytotoxic lipid, galactosylsphingosine...

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Detalhes bibliográficos
Main Authors: Reddy, Adarsh S., Patel, Jigisha R., Vogler, Carole, Klein, Robyn S., Sands, Mark S.
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2013
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3670857/
https://ncbi.nlm.nih.gov/pubmed/23755134
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0064647
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