Mutations in NYX , encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness
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There was an error in the printed version of Fig. 5c. The correct figure is shown below.
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Erratum. Nat Genet 27, 125 (2001). https://doi.org/10.1038/83693
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DOI: https://doi.org/10.1038/83693
