Circulating microRNAs in Fabry Disease

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 quality of lif...

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Detalles Bibliográficos
Autores principales: Xiao, Ke, Lu, Dongchao, Hoepfner, Jeannine, Santer, Laura, Gupta, Shashi, Pfanne, Angelika, Thum, Sabrina, Lenders, Malte, Brand, Eva, Nordbeck, Peter, Thum, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6813291/
https://www.ncbi.nlm.nih.gov/pubmed/31649303
http://dx.doi.org/10.1038/s41598-019-51805-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6813291/
https://www.ncbi.nlm.nih.gov/pubmed/31649303
http://dx.doi.org/10.1038/s41598-019-51805-6

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