Lipid and energy metabolism in Wilson disease()

Copper accumulation and deficiency are reciprocally connected to lipid metabolism. In Wilson disease (WD), which is caused by a genetic loss of function of the copper-transporting P-type ATPase beta, copper accumulates mainly in the liver and lipid metabolism is dysregulated. The underlying mechanis...

Descripción completa

Detalles Bibliográficos
Autores principales: Mazi, Tagreed A., Shibata, Noreene M., Medici, Valentina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7437987/
https://www.ncbi.nlm.nih.gov/pubmed/32832193
http://dx.doi.org/10.1016/j.livres.2020.02.002

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7437987/
https://www.ncbi.nlm.nih.gov/pubmed/32832193
http://dx.doi.org/10.1016/j.livres.2020.02.002

Ejemplares similares