[cite web | title = Entrez Gene: FRMD7 FERM domain containing 7| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=90167| accessdate = ] ] PBB_Summary
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References
Further reading
PBB_Further_reading
citations =
*cite journal | author=Gutmann DH, Brooks ML, Emanuel BS, "et al." |title=Congenital nystagmus in a (46,XX/45,X) mosaic woman from a family with X-linked congenital nystagmus. |journal=Am. J. Med. Genet. |volume=39 |issue= 2 |pages= 167–9 |year= 1991 |pmid= 2063919 |doi= 10.1002/ajmg.1320390210
*cite journal | author=Cabot A, Rozet JM, Gerber S, "et al." |title=A gene for X-linked idiopathic congenital nystagmus (NYS1) maps to chromosome Xp11.4-p11.3. |journal=Am. J. Hum. Genet. |volume=64 |issue= 4 |pages= 1141–6 |year= 2000 |pmid= 10090899 |doi=
*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=Ota T, Suzuki Y, Nishikawa T, "et al." |title=Complete sequencing and characterization of 21,243 full-length human cDNAs. |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40–5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285
*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=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=Guo X, Li S, Jia X, "et al." |title=Linkage analysis of two families with X-linked recessive congenital motor nystagmus. |journal=J. Hum. Genet. |volume=51 |issue= 1 |pages= 76–80 |year= 2006 |pmid= 16240070 |doi= 10.1007/s10038-005-0316-y
*cite journal | author=Tarpey P, Thomas S, Sarvananthan N, "et al." |title=Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus. |journal=Nat. Genet. |volume=38 |issue= 11 |pages= 1242–4 |year= 2007 |pmid= 17013395 |doi= 10.1038/ng1893
*cite journal | author=Schorderet DF, Tiab L, Gaillard MC, "et al." |title=Novel mutations in FRMD7 in X-linked congenital nystagmus. Mutation in brief #963. Online. |journal=Hum. Mutat. |volume=28 |issue= 5 |pages= 525 |year= 2007 |pmid= 17397053 |doi= 10.1002/humu.9492
*cite journal | author=Zhang Q, Xiao X, Li S, Guo X |title=FRMD7 mutations in Chinese families with X-linked congenital motor nystagmus. |journal=Mol. Vis. |volume=13 |issue= |pages= 1375–8 |year= 2007 |pmid= 17768376 |doi=
*cite journal | author=Self JE, Shawkat F, Malpas CT, "et al." |title=Allelic variation of the FRMD7 gene in congenital idiopathic nystagmus. |journal=Arch. Ophthalmol. |volume=125 |issue= 9 |pages= 1255–63 |year= 2007 |pmid= 17846367 |doi= 10.1001/archopht.125.9.1255
*cite journal | author=Zhang B, Liu Z, Zhao G, "et al." |title=Novel mutations of the FRMD7 gene in X-linked congenital motor nystagmus. |journal=Mol. Vis. |volume=13 |issue= |pages= 1674–9 |year= 2007 |pmid= 17893669 |doi=
*cite journal | author=Kaplan Y, Vargel I, Kansu T, "et al." |title=Skewed X inactivation in an X linked nystagmus family resulted from a novel, p.R229G, missense mutation in the FRMD7 gene. |journal=The British journal of ophthalmology |volume=92 |issue= 1 |pages= 135–41 |year= 2008 |pmid= 17962394 |doi= 10.1136/bjo.2007.128157
*cite journal | author=Shiels A, Bennett TM, Prince JB, Tychsen L |title=X-linked idiopathic infantile nystagmus associated with a missense mutation in FRMD7. |journal=Mol. Vis. |volume=13 |issue= |pages= 2233–41 |year= 2008 |pmid= 18087240 |doi=
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