Mutations in NYX , encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness

    N T Bech-Hansen et al.

    Nature Genet. 26, 319– 323 (2000).

    There was an error in the printed version of Fig. 5c. The correct figure is shown below.

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    The online version of the original article can be found at 10.1038/81619

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    Erratum. Nat Genet 27, 125 (2001) doi:10.1038/83693

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