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Article

Role of genotyping in Wilson’s disease

5 Dec 2008

Abstract excerpt

The molecular characterization of hereditary diseases has given rise to major advancements in the understanding of pathophysiology in human disease. Among these inborn defects of metabolism, Wilson’s disease (WD) serves as an excellent model to study processes such as copper metabolism, oxidative stress, neurodegeneration, psychiatric disease, acute and chronic liver failure, as well as hepatocarcinogenesis. WD...

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PMID: 19118916
DOI: 10.1016/j.jhep.2008.11.008

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