The world's first wiki where authorship really matters (Nature Genetics, 2008). Due credit and reputation for authors. Imagine a global collaborative knowledge base for original thoughts. Search thousands of articles and collaborate with scientists around the globe.

wikigene or wiki gene protein drug chemical gene disease author authorship tracking collaborative publishing evolutionary knowledge reputation system wiki2.0 global collaboration genes proteins drugs chemicals diseases compound
Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 
Gene Review

OASD  -  ocular albinism and sensorineural deafness

Homo sapiens

 
 
Welcome! If you are familiar with the subject of this article, you can contribute to this open access knowledge base by deleting incorrect information, restructuring or completely rewriting any text. Read more.
 

Disease relevance of OASD

  • X-linked ocular albinism with late-onset sensorineural deafness (OASD) is an autonomous disorder that poses significant clinical problems, causing affected individuals to be blind and deaf by early middle age [1].
 

High impact information on OASD

  • In the present report, a large South African family with OASD was investigated at the molecular level and tight linkage was found to the DXS452 locus at Xp22.3 using 25 informative meioses, with a maximum lod score of 7.1 at a recombination fraction of 0.00 [1].
  • We have investigated a large Afrikaner kindred in which seven males had ocular albinism and late-onset sensorineural deafness (OASD) [2].

References

  1. X-linked ocular albinism and sensorineural deafness: linkage to Xp22.3. Winship, I.M., Babaya, M., Ramesar, R.S. Genomics (1993) [Pubmed]
  2. X-linked inheritance of ocular albinism with late-onset sensorineural deafness. Winship, I., Gericke, G., Beighton, P. Am. J. Med. Genet. (1984) [Pubmed]
 
WikiGenes - Universities