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We aim to understand the molecular basis and pathophysiology of human diseases as a prerequisite to develop novel therapeutic interventions.
- Identification of new genes and mutations in human diseases
- Characterization of gene function in normal physiology and disease
- Functional analyses of mutations at the molecular level
- Development of therapeutic treatment approaches for genetic diseases
We are very grateful to all patients and their families as well as various patient organizations for their tremendous support of our research activities.
EMDO Stiftung
Hartmann Müller Stiftung
Novartis Stiftung
Olga Mayenfisch Stiftung
Retina Suisse
Schweizerische Herzstiftung
Schweizerischer Fonds zur Verhütung und Bekämpfung von Blindheit
Schweizerischer Nationalfonds (SNF)
Universität Zürich (Forschungskredit)
Dr. Werner Jackstädt Stiftung
Velux Stiftung