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Gene Review

USH2B  -  Usher syndrome 2B (autosomal recessive, mild)

Homo sapiens

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Disease relevance of USH2B

 

High impact information on USH2B

  • This maps the gene underlying USH2B to a chromosomal region which overlaps the interval defined for the non-syndromic sensorineural recessive deafness DFNB6, raising the possibility that a single gene underlies both defects [1].
 

Other interactions of USH2B

  • However, the audiometric features in the patients affected by USH2B and DFNB6 are very different [1].

References

  1. A novel locus for Usher syndrome type II, USH2B, maps to chromosome 3 at p23-24.2. Hmani, M., Ghorbel, A., Boulila-Elgaied, A., Ben Zina, Z., Kammoun, W., Drira, M., Chaabouni, M., Petit, C., Ayadi, H. Eur. J. Hum. Genet. (1999) [Pubmed]
 
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