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Cone dystrophy with supernormal rod response is strictly associated with mutations in KCNV2. [electronic resource] by
- Wissinger, Bernd
- Dangel, Susann
- Jägle, Herbert
- Hansen, Lars
- Baumann, Britta
- Rudolph, Günther
- Wolf, Christiane
- Bonin, Michael
- Koeppen, Katja
- Ladewig, Thomas
- Kohl, Susanne
- Zrenner, Eberhart
- Rosenberg, Thomas
Producer: 20080313
In:
Investigative ophthalmology & visual science vol. 49
Availability: No items available.
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