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Wilson’s disease: Prospective developments towards new therapies
Wilson’s disease (WD) is an autosomal recessive disorder of copper metabolism, caused by mutations in the ATP7B gene. A clear demand for novel WD treatment strategies has emerged. Although therapies using zinc salts and copper chelators can effectively cure WD, these drugs exhibit limitations in a s...
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| Publicado no: | World J Gastroenterol |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Baishideng Publishing Group Inc
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5558108/ https://ncbi.nlm.nih.gov/pubmed/28852304 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3748/wjg.v23.i30.5451 |
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