Grantee
Kim Fabiano Marquart
Nerai Bioscience
This project combines artificial intelligence with high-throughput directed evolution to engineer customized CRISPR gene-editing tools that can target disease mutations currently unreachable with existing methods. With initial applications in rare metabolic and liver disorders such as citrullinemia type I and phenylketonuria, the work aims to expand patient access to first-in-class genome medicines.
Key Facts
- Country
Switzerland
- University
University of Zurich
- Year
2026


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