Copper and Trace Elements in Gallbladder form Patients with Wilson’s Disease Imaged and Determined by Synchrotron X-ray Fluorescence

Investigations about suspected tissue alterations and the role of gallbladder in Wilson’s disease (WD)—an inherited genetic disease with impaired copper metabolism—are rare. Therefore, tissue from patients with genetically characterised WD was investigated by microscopic synchrotron X-ray fluorescen...

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Detalles Bibliográficos
Autores principales: Osterode, Wolf, Falkenberg, Gerald, Wrba, Fritz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8705686/
https://www.ncbi.nlm.nih.gov/pubmed/34940728
http://dx.doi.org/10.3390/jimaging7120261

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8705686/
https://www.ncbi.nlm.nih.gov/pubmed/34940728
http://dx.doi.org/10.3390/jimaging7120261

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