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An assessment of prevalence of Type 1 CFI rare variants in European AMD, and why lack of broader genetic data hinders development of new treatments and healthcare access
- Amy V. Jones,
- Darin Curtiss,
- Claire Harris,
- Tom Southerington,
- Marco Hautalahti,
- Pauli Wihuri,
- Johanna Mäkelä,
- Roosa E. Kallionpää,
- Enni Makkonen,
- Theresa Knopp
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- Published: September 6, 2022
- https://doi.org/10.1371/journal.pone.0272260