Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
4004681 | American Journal of Ophthalmology | 2009 | 14 Pages |
Abstract
This series describes the broad spectrum of phenotypes associated with PRPH2 mutations. FAF and OCT are helpful tools for diagnosis and evaluation of disease progression. We report novel PRPH2 mutations in patients with CACD, CRD, and adRP.
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Authors
Agnes B. Renner, Britta S. Fiebig, Bernhard H.F. Weber, Bernd Wissinger, Sten Andreasson, Andreas Gal, Elke Cropp, Susanne Kohl, Ulrich Kellner,