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Development of a model system for neuronal dysfunction in Fabry Disease

Fabry disease is a glycosphingolipid storage disorder that is caused by a genetic deficiency of the enzyme alpha-galactosidase A (AGA, EC 3.2.1.22). It is a multisystem disease that affects the vascular, cardiac, renal, and nervous systems. One of the hallmarks of this disorder is neuropathic pain a...

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Bibliographic Details
Published in:Mol Genet Metab
Main Authors: Kaneski, Christine R., Brady, Roscoe O., Hanover, John A., Schueler, Ulrike H.
Format: Artigo
Language:Inglês
Published: 2016
Subjects:
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC5031533/
https://ncbi.nlm.nih.gov/pubmed/27471012
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymgme.2016.07.010
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