Wilson’s Disease—Genetic Puzzles with Diagnostic Implications
(1) Introduction: Wilson’s disease (WND) is an autosomal recessive disorder of copper metabolism. The WND gene is <i>ATP7B</i>, located on chromosome 13. WND is characterized by high clinical variability, which causes diagnostic difficulties. (2) Methods: The PubMed, Science Direct, and Wiley Online...
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| Principais autores: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
MDPI AG
2023-03-01
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| coleção: | Diagnostics |
| Assuntos: | |
| Acesso em linha: | https://www.mdpi.com/2075-4418/13/7/1287 |
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