Expression of Ripk1 and DAM genes correlates with severity and progression of Krabbe disease

Krabbe disease, an inherited leukodystrophy, is a sphingolipidosis caused by deficiency of β-galactocerebrosidase: it is characterized by myelin loss, and pathological activation of macrophage/microglia and astrocytes. To define driving pathogenic factors, we explored the expression repertoire of ca...

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Detalles Bibliográficos
Autores principales: Cachón-González, María B, Wang, Susan, Cox, Timothy M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
General Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8561423/
https://www.ncbi.nlm.nih.gov/pubmed/34172992
http://dx.doi.org/10.1093/hmg/ddab159

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8561423/
https://www.ncbi.nlm.nih.gov/pubmed/34172992
http://dx.doi.org/10.1093/hmg/ddab159

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