Circulating microRNAs in Fabry Disease

Abstract Fabry disease is an X-linked deficiency of the lysosomal hydrolase alpha-galactosidase A (alpha-Gal). This results in an accumulation of globotriaosylceramide (GL-3/Gb3) in a variety of cells with subsequent functional impairment. The continuous progress of FD often leads to decreased quali...

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Autores principales: Ke Xiao, Dongchao Lu, Jeannine Hoepfner, Laura Santer, Shashi Gupta, Angelika Pfanne, Sabrina Thum, Malte Lenders, Eva Brand, Peter Nordbeck, Thomas Thum
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2019
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Acceso en línea:https://doaj.org/article/875154d0910d4335b4c8cf600b0c2de4
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