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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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| Publicado no: | JIMD Rep |
|---|---|
| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer Berlin Heidelberg
2015
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| 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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