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Management Perspective of Wilson’s Disease: Early Diagnosis and Individualized Therapy
Wilson’s disease (WD) is an inherited disease caused by mutations in ATP7B and is characterized by the pathological accumulation of copper in the liver and brain. Common clinical manifestations of WD include a wide range of liver disease and neurological symptoms. In some patients, psychiatric sympt...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Bentham Science Publishers
2021
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8206458/ https://www.ncbi.nlm.nih.gov/pubmed/32351182 http://dx.doi.org/10.2174/1570159X18666200429233517 |