FRMD7

WikiDoc Resources for FRMD7
Articles
Most recent articles on FRMD7 Most cited articles on FRMD7 Review articles on FRMD7 Articles on FRMD7 in N Eng J Med, Lancet, BMJ
Media
Powerpoint slides on FRMD7 Images of FRMD7 Photos of FRMD7 Podcasts & MP3s on FRMD7 Videos on FRMD7
Evidence Based Medicine
Cochrane Collaboration on FRMD7 Bandolier on FRMD7 TRIP on FRMD7
Clinical Trials
Ongoing Trials on FRMD7 at Clinical Trials.gov Trial results on FRMD7 Clinical Trials on FRMD7 at Google
Guidelines / Policies / Govt
US National Guidelines Clearinghouse on FRMD7 NICE Guidance on FRMD7 NHS PRODIGY Guidance FDA on FRMD7 CDC on FRMD7
Books
Books on FRMD7
News
FRMD7 in the news Be alerted to news on FRMD7 News trends on FRMD7
Commentary
Blogs on FRMD7
Definitions
Definitions of FRMD7
Patient Resources / Community
Patient resources on FRMD7 Discussion groups on FRMD7 Patient Handouts on FRMD7 Directions to Hospitals Treating FRMD7 Risk calculators and risk factors for FRMD7
Healthcare Provider Resources
Symptoms of FRMD7 Causes & Risk Factors for FRMD7 Diagnostic studies for FRMD7 Treatment of FRMD7
Continuing Medical Education (CME)
CME Programs on FRMD7
International
FRMD7 en Espanol FRMD7 en Francais
Business
FRMD7 in the Marketplace Patents on FRMD7
Experimental / Informatics
List of terms related to FRMD7

FERM domain containing 7, also known as FRMD7, is a human gene.

Further reading

• Gutmann DH, Brooks ML, Emanuel BS; et al. (1991). "Congenital nystagmus in a (46,XX/45,X) mosaic woman from a family with X-linked congenital nystagmus". Am. J. Med. Genet. 39 (2): 167–9. doi:10.1002/ajmg.1320390210. PMID 2063919.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Cabot A, Rozet JM, Gerber S; et al. (2000). "A gene for X-linked idiopathic congenital nystagmus (NYS1) maps to chromosome Xp11.4-p11.3". Am. J. Hum. Genet. 64 (4): 1141–6. PMID 10090899.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Strausberg RL, Feingold EA, Grouse LH; et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMID 12477932.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Ota T, Suzuki Y, Nishikawa T; et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Gerhard DS, Wagner L, Feingold EA; et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMID 15489334.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Ross MT, Grafham DV, Coffey AJ; et al. (2005). "The DNA sequence of the human X chromosome". Nature. 434 (7031): 325–37. doi:10.1038/nature03440. PMID 15772651.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Guo X, Li S, Jia X; et al. (2006). "Linkage analysis of two families with X-linked recessive congenital motor nystagmus". J. Hum. Genet. 51 (1): 76–80. doi:10.1007/s10038-005-0316-y. PMID 16240070.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Tarpey P, Thomas S, Sarvananthan N; et al. (2007). "Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus". Nat. Genet. 38 (11): 1242–4. doi:10.1038/ng1893. PMID 17013395.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Schorderet DF, Tiab L, Gaillard MC; et al. (2007). "Novel mutations in FRMD7 in X-linked congenital nystagmus. Mutation in brief #963. Online". Hum. Mutat. 28 (5): 525. doi:10.1002/humu.9492. PMID 17397053.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Zhang Q, Xiao X, Li S, Guo X (2007). "FRMD7 mutations in Chinese families with X-linked congenital motor nystagmus". Mol. Vis. 13: 1375–8. PMID 17768376.CS1 maint: Multiple names: authors list (link)
• Self JE, Shawkat F, Malpas CT; et al. (2007). "Allelic variation of the FRMD7 gene in congenital idiopathic nystagmus". Arch. Ophthalmol. 125 (9): 1255–63. doi:10.1001/archopht.125.9.1255. PMID 17846367.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Zhang B, Liu Z, Zhao G; et al. (2007). "Novel mutations of the FRMD7 gene in X-linked congenital motor nystagmus". Mol. Vis. 13: 1674–9. PMID 17893669.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Kaplan Y, Vargel I, Kansu T; et al. (2008). "Skewed X inactivation in an X linked nystagmus family resulted from a novel, p.R229G, missense mutation in the FRMD7 gene". The British journal of ophthalmology. 92 (1): 135–41. doi:10.1136/bjo.2007.128157. PMID 17962394.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Shiels A, Bennett TM, Prince JB, Tychsen L (2008). "X-linked idiopathic infantile nystagmus associated with a missense mutation in FRMD7". Mol. Vis. 13: 2233–41. PMID 18087240.CS1 maint: Multiple names: authors list (link)