CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia (Q34385718)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia |
scientific article |
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CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia (English)
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Dorit Lev
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Richard G Weleber
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Bernd Wissinger
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Susanne Kohl
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Balazs Varsanyi
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Gesine Abadin Antunes
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Britta Baumann
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Carel B Hoyng
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Herbert Jägle
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Thomas Rosenberg
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Ulrich Kellner
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Birgit Lorenz
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Roberto Salati
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Bernhard Jurklies
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Agnes Farkas
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Sten Andreasson
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Samuel G Jacobson
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Günther Rudolph
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Claudio Castellan
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Helene Dollfus
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Eric Legius
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Mario Anastasi
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Pierre Bitoun
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Paul A Sieving
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Francis L Munier
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Eberhart Zrenner
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Lindsay T Sharpe
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Frans P M Cremers
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1 March 2005
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302-308
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