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Increased expression of Trpv1 in peripheral terminals mediates thermal nociception in Fabry disease mouse model
Fabry disease is a X-linked lysosomal storage disorder caused by deficient function of the alpha-galactosidase A (α-GalA) enzyme. α-GalA deficiency leads to multisystemic clinical manifestations caused by the preferential accumulation of globotriaosylceramide (Gb3) in the endothelium and vascular sm...
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| Udgivet i: | Mol Pain |
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| Main Authors: | , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
SAGE Publications
2016
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5009828/ https://ncbi.nlm.nih.gov/pubmed/27531673 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/1744806916663729 |
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