[cite web | title = Entrez Gene: NYX nyctalopin| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=60506| accessdate = ] ] PBB_Summary
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References
Further reading
PBB_Further_reading
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*cite journal | author=Musarella MA, Weleber RG, Murphey WH, "et al." |title=Assignment of the gene for complete X-linked congenital stationary night blindness (CSNB1) to Xp11.3. |journal=Genomics |volume=5 |issue= 4 |pages= 727–37 |year= 1990 |pmid= 2574143 |doi=
*cite journal | author=Hardcastle AJ, David-Gray ZK, Jay M, "et al." |title=Localization of CSNBX (CSNB4) between the retinitis pigmentosa loci RP2 and RP3 on proximal Xp. |journal=Invest. Ophthalmol. Vis. Sci. |volume=38 |issue= 13 |pages= 2750–5 |year= 1998 |pmid= 9418727 |doi=
*cite journal | author=Bech-Hansen NT, Naylor MJ, Maybaum TA, "et al." |title=Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness. |journal=Nat. Genet. |volume=26 |issue= 3 |pages= 319–23 |year= 2000 |pmid= 11062471 |doi= 10.1038/81619
*cite journal | author=Pusch CM, Zeitz C, Brandau O, "et al." |title=The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein. |journal=Nat. Genet. |volume=26 |issue= 3 |pages= 324–7 |year= 2000 |pmid= 11062472 |doi= 10.1038/81627
*cite journal | author=Jacobi FK, Andréasson S, Langrova H, "et al." |title=Phenotypic expression of the complete type of X-linked congenital stationary night blindness in patients with different mutations in the NYX gene. |journal=Graefes Arch. Clin. Exp. Ophthalmol. |volume=240 |issue= 10 |pages= 822–8 |year= 2003 |pmid= 12397430 |doi= 10.1007/s00417-002-0562-z
*cite journal | author=Strausberg RL, Feingold EA, Grouse LH, "et al." |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899
*cite journal | author=Gregg RG, Mukhopadhyay S, Candille SI, "et al." |title=Identification of the gene and the mutation responsible for the mouse nob phenotype. |journal=Invest. Ophthalmol. Vis. Sci. |volume=44 |issue= 1 |pages= 378–84 |year= 2003 |pmid= 12506099 |doi=
*cite journal | author=Zito I, Allen LE, Patel RJ, "et al." |title=Mutations in the CACNA1F and NYX genes in British CSNBX families. |journal=Hum. Mutat. |volume=21 |issue= 2 |pages= 169 |year= 2003 |pmid= 12552565 |doi= 10.1002/humu.9106
*cite journal | author=Zeitz C, Scherthan H, Freier S, "et al." |title=NYX (nyctalopin on chromosome X), the gene mutated in congenital stationary night blindness, encodes a cell surface protein. |journal=Invest. Ophthalmol. Vis. Sci. |volume=44 |issue= 10 |pages= 4184–91 |year= 2003 |pmid= 14507859 |doi=
*cite journal | author=Khan NW, Kondo M, Hiriyanna KT, "et al." |title=Primate Retinal Signaling Pathways: Suppressing ON-Pathway Activity in Monkey With Glutamate Analogues Mimics Human CSNB1-NYX Genetic Night Blindness. |journal=J. Neurophysiol. |volume=93 |issue= 1 |pages= 481–92 |year= 2005 |pmid= 15331616 |doi= 10.1152/jn.00365.2004
*cite journal | author=Gerhard DS, Wagner L, Feingold EA, "et al." |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504
*cite journal | author=Zeitz C, Minotti R, Feil S, "et al." |title=Novel mutations in CACNA1F and NYX in Dutch families with X-linked congenital stationary night blindness. |journal=Mol. Vis. |volume=11 |issue= |pages= 179–83 |year= 2005 |pmid= 15761389 |doi=
*cite journal | author=Ross MT, Grafham DV, Coffey AJ, "et al." |title=The DNA sequence of the human X chromosome. |journal=Nature |volume=434 |issue= 7031 |pages= 325–37 |year= 2005 |pmid= 15772651 |doi= 10.1038/nature03440
*cite journal | author=Morgans CW, Ren G, Akileswaran L |title=Localization of nyctalopin in the mammalian retina. |journal=Eur. J. Neurosci. |volume=23 |issue= 5 |pages= 1163–71 |year= 2006 |pmid= 16553780 |doi= 10.1111/j.1460-9568.2006.04647.x
*cite journal | author=Xiao X, Jia X, Guo X, "et al." |title=CSNB1 in Chinese families associated with novel mutations in NYX. |journal=J. Hum. Genet. |volume=51 |issue= 7 |pages= 634–40 |year= 2006 |pmid= 16670814 |doi= 10.1007/s10038-006-0406-5
*cite journal | author=Zhang Q, Xiao X, Li S, "et al." |title=Mutations in NYX of individuals with high myopia, but without night blindness. |journal=Mol. Vis. |volume=13 |issue= |pages= 330–6 |year= 2007 |pmid= 17392683 |doi=
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