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Wilson's Disease: Diagnosis of Wilson's Disease in Ethiopian Young Sisters
BACKGROUND: Wilson's disease is an inherited autosomal recessive disorder of copper metabolism. Clinical signs, biochemical parameters, histologic findings, and/or ATP7B genetic testing are required to diagnose Wilson's disease. Case Presentation. 25-year-old and 22-year-old young women (s...
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| Publicado no: | Case Rep Med |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Hindawi
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7396006/ https://ncbi.nlm.nih.gov/pubmed/32774387 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2020/7650170 |
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