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.
The online version of the original article can be found at 10.1038/81619
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Has the 'Silver Thread' of the Criminal Law Lost its Lustre? The Modern Prosecutor as a Minister of Justice
SSRN Electronic Journal (2012)