Human kidney organoids reveal the role of glutathione in Fabry disease

Fabry disease is an X-linked lysosomal storage disease caused by a mutation in the galactosidase alpha (GLA) gene. Despite advances in therapeutic technologies, the lack of humanized experimental models of Fabry disease has limited the development of new therapies to cure the disease. Herein, we mod...

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Detalles Bibliográficos
Autores principales: Kim, Jin Won, Kim, Hyung Wook, Nam, Sun Ah, Lee, Jong Young, Cho, Hae Jin, Kim, Tae-Min, Kim, Yong Kyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8568890/
https://www.ncbi.nlm.nih.gov/pubmed/34654880
http://dx.doi.org/10.1038/s12276-021-00683-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8568890/
https://www.ncbi.nlm.nih.gov/pubmed/34654880
http://dx.doi.org/10.1038/s12276-021-00683-y

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