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Therapeutic strategies in Wilson disease: pathophysiology and mode of action
Wilson disease is a copper overload disease treatable with the chelators D-penicillamine and trientine to enhance urinary excretion or with zinc which predominantly inhibits absorption. By lifelong treatment a normal life expectancy and significant improvement of hepatic injury as well as neurologic...
Autores principales: | Stremmel, Wolfgang, Weiskirchen, Ralf |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8106045/ https://www.ncbi.nlm.nih.gov/pubmed/33987430 http://dx.doi.org/10.21037/atm-20-3090 |
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