Color Vision Defects

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Solaki, M., Baumann, B., Reuter, P., Andreasson, S., Audo, I., Ayuso, C., Balousha, G., Benedicenti, F., Birch, D., Bitoun, P., Blain, D., Bocquet, B., Branham, K., Català‐Mora, J., De Baere, E., Dollfus, H., Falana, M., Giorda, R., Golovleva, I., … Kohl, S. (2022). Comprehensive variant spectrum of the CNGA3 gene in patients affected by achromatopsia. Human Mutation, 43(7), 832–858. Portico. https://doi.org/10.1002/humu.24371
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