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CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia. [electronic resource] by
- Kohl, Susanne
- Varsanyi, Balazs
- Antunes, Gesine Abadin
- Baumann, Britta
- Hoyng, Carel B
- Jägle, Herbert
- Rosenberg, Thomas
- Kellner, Ulrich
- Lorenz, Birgit
- Salati, Roberto
- Jurklies, Bernhard
- Farkas, Agnes
- Andreasson, Sten
- Weleber, Richard G
- Jacobson, Samuel G
- Rudolph, Günther
- Castellan, Claudio
- Dollfus, Helene
- Legius, Eric
- Anastasi, Mario
- Bitoun, Pierre
- Lev, Dorit
- Sieving, Paul A
- Munier, Francis L
- Zrenner, Eberhart
- Sharpe, Lindsay T
- Cremers, Frans P M
- Wissinger, Bernd
Producer: 20050712
In:
European journal of human genetics : EJHG vol. 13
Availability: No items available.
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