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

Reference

Bech-Hansen, N.Torben, et al. “Mutations in NYX, Encoding the Leucine-Rich Proteoglycan Nyctalopin, Cause X-Linked Complete Congenital Stationary Night Blindness”. Nature Genetics, vol. 26, no. 3, Oct. 2000, pp. 319–323, https://doi.org/10.1038/81619.

PubMed Reference Number (PMID)

11062471