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The dilemma to diagnose Wilson disease by genetic testing alone
BACKGROUND: Wilson disease (WD) is an autosomal recessive disorder of hepatic copper excretion. About sixty per cent of patients present with liver disease. WD is considered a fatal disease if undiagnosed and/or untreated but recent data indicate that disease penetrance may not be 100%. MATERIALS AN...
Autores principales: | Stättermayer, Albert Friedrich, Entenmann, Andreas, Gschwantler, Michael, Zoller, Heinz, Hofer, Harald, Ferenci, Peter |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6772051/ https://www.ncbi.nlm.nih.gov/pubmed/31169307 http://dx.doi.org/10.1111/eci.13147 |
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