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Innate and Adaptive Immune Response in Fabry Disease

Fabry disease is an X-linked lysosomal storage disease in which mutations of the gene (GLA) cause a deficiency of the lysosomal hydrolase α-galactosidase A (α-Gal). This defect results in an accumulation of glycosphingolipids, primarily globotriaosylceramide (Gb3) which causes a multisystemic vascul...

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Detalhes bibliográficos
Publicado no:JIMD Rep
Main Authors: Mauhin, Wladimir, Lidove, Olivier, Masat, Elisa, Mingozzi, Federico, Mariampillai, Kuberaka, Ziza, Jean-Marc, Benveniste, Olivier
Formato: Artigo
Idioma:Inglês
Publicado em: Springer Berlin Heidelberg 2015
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4486269/
https://ncbi.nlm.nih.gov/pubmed/25690728
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/8904_2014_371
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