CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia
Open Access
- 15 December 2004
- journal article
- research article
- Published by Springer Science and Business Media LLC in European Journal of Human Genetics
- Vol. 13 (3), 302-308
- https://doi.org/10.1038/sj.ejhg.5201269
Abstract
No abstract availableKeywords
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