The molecular genetics of Usher syndrome.

@article{Ahmed2003TheMG,
  title={The molecular genetics of Usher syndrome.},
  author={Zubair M Ahmed and Shiekh Riazuddin and E. R. Wilcox},
  journal={Clinical genetics},
  year={2003},
  volume={63 6},
  pages={
          431-44
        }
}
Association of sensorineural deafness and progressive retinitis pigmentosa with and without a vestibular abnormality is the hallmark of Usher syndrome and involves at least 12 loci among three different clinical subtypes. Genes identified for the more commonly inherited loci are USH2A (encoding usherin), MYO7A (encoding myosin VIIa), CDH23 (encoding cadherin 23), PCDH15 (encoding protocadherin 15), USH1C (encoding harmonin), USH3A (encoding clarin 1), and USH1G (encoding SANS). Transcripts from… CONTINUE READING
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