CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia
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| Description | scientific article |
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author: Dorit Lev Paul Sieving Bernd Wissinger Carel B Hoyng Richard G Weleber |
| Publication date | March 1, 2005 |
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| Missing/wrong data? | Edit Wikidata item |