Dysregulated autophagy contributes to podocyte damage in Fabry's disease.

Dysregulated autophagy contributes to podocyte damage in Fabry's disease.

Fabry's disease results from an inborn error of glycosphingolipid metabolism that is due to deficiency of the lysosomal hydrolase α-galactosidase A. This X-linked defect results in the accumulation of enzyme substrates with terminally α-glycosidically bound galactose, mainly the neutral glycosp...

Full description

Bibliographic Details
Main Authors: Max C Liebau, Fabian Braun, Katja Höpker, Claudia Weitbrecht, Valerie Bartels, Roman-Ulrich Müller, Susanne Brodesser, Moin A Saleem, Thomas Benzing, Bernhard Schermer, Markus Cybulla, Christine E Kurschat
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23691056/?tool=EBI

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23691056/?tool=EBI

Similar Items