USH2A

From Wikipedia, the free encyclopedia

This is an old revision of this page, as edited by 205.152.158.201 (talk) at 17:00, 3 August 2010 (Added external link to GeneReviews/NCBI/NIH/UW entry on Usher Syndrome Type II). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Template:PBB Usherin is a protein that in humans is encoded by the USH2A gene.[1][2]

Template:PBB Summary

External Links

References

  1. ^ Eudy JD, Weston MD, Yao S, Hoover DM, Rehm HL, Ma-Edmonds M, Yan D, Ahmad I, Cheng JJ, Ayuso C, Cremers C, Davenport S, Moller C, Talmadge CB, Beisel KW, Tamayo M, Morton CC, Swaroop A, Kimberling WJ, Sumegi J (1998). "Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa". Science. 280 (5370): 1753–7. doi:10.1126/science.280.5370.1753. PMID 9624053. {{cite journal}}: Unknown parameter |month= ignored (help)CS1 maint: multiple names: authors list (link)
  2. ^ Weston MD, Eudy JD, Fujita S, Yao S, Usami S, Cremers C, Greenberg J, Ramesar R, Martini A, Moller C, Smith RJ, Sumegi J, Kimberling WJ (2000). "Genomic structure and identification of novel mutations in usherin, the gene responsible for Usher syndrome type IIa". Am J Hum Genet. 66 (4): 1199–210. doi:10.1086/302855. PMC 1288187. PMID 10729113. {{cite journal}}: Unknown parameter |month= ignored (help)CS1 maint: multiple names: authors list (link)

Further reading

Template:PBB Controls