CellWell record HH-457736
From Copper Accumulation to Personalized Medicine: Understanding Wilson Disease and Looking Ahead to Future Directions
Chenyu Zhang
GBP Proceedings Series ยท 2026
In plain language
This review linked copper accumulation from ATP7B loss-of-function mutations to oxidative damage and liver fibrosis, and discussed gene therapy and newborn screening as emerging options for Wilson disease.
- Evidence
- Emerging
- Design
- Primary research (design unspecified)
Cite this record: https://thecellwell.org/studies/HH-457736
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