Intestinal expression of metal transporters in Wilson’s disease

In Wilson’s disease (WND), biallelic ATP7B gene mutation is responsible for pathological copper accumulation in the liver, brain and other organs. It has been proposed that copper transporter 1 (CTR1) and the divalent metal transporter 1 (DMT1) translocate copper across the human intestinal epitheli...

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Detalles Bibliográficos
Autores principales: Przybyłkowski, Adam, Gromadzka, Grażyna, Wawer, Adriana, Grygorowicz, Tomasz, Cybulska, Anna, Członkowska, Anna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2013
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3825560/
https://www.ncbi.nlm.nih.gov/pubmed/23963605
http://dx.doi.org/10.1007/s10534-013-9668-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3825560/
https://www.ncbi.nlm.nih.gov/pubmed/23963605
http://dx.doi.org/10.1007/s10534-013-9668-5

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