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Substrate-specific gene expression profiles in different kidney cell types are associated with Fabry disease
Fabry disease is an X-linked lysosomal storage disorder caused by mutations in the gene encoding the α-galactosidase A (α-Gal A) lysosomal enzyme, which results in globotriaosylceramide (Gb3) storage in vascular endothelial cells and different cell types throughout the body. Involvement of the of Fa...
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| Publicado no: | Mol Med Rep |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
D.A. Spandidos
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4581816/ https://ncbi.nlm.nih.gov/pubmed/26135632 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/mmr.2015.4010 |
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