CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia

Susanne Kohl, Balazs Varsanyi, Gesine Abadin Antunes, Britta Baumann, Carel B. Hoyng, Herbert Jägle, Thomas Rosenberg, Ulrich Kellner, Birgit Lorenz, Roberto Salati, Bernhard Jurklies, Agnes Farkas, Sten Andreasson, Richard G. Weleber, Samuel G. Jacobson, Günther Rudolph, Claudio Castellan, Helene Dollfus, Eric Legius, Mario AnastasiPierre Bitoun, Dorit Lev, Paul A. Sieving, Francis L. Munier, Eberhart Zrenner, Lindsay T. Sharpe, Frans P.M. Cremers, Bernd Wissinger

Research output: Contribution to journal › Article › peer-review

201 Scopus citations

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Medicine & Life Sciences