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  1. Home
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  3. usher syndrome
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  • MYO7A gene

  • USH1G gene

  • CDH23 gene

  • CIB2 gene

  • USH1C gene

  • PCDH15 gene

  • Usher syndrome: for professionals

    Usher syndrome is a group of inherited disorders characterised by a combination of sensorineural hearing loss and retinitis pigmentosa.
  • Usher syndrome: for patients

    Usher syndrome is a group of inherited disorders characterised by a combination of hearing loss and visual impairment due to retinitis pigmentosa.
  • RNA therapy

    RNA is involved in protein production from DNA in human cells. Mutations in DNA can be passed down to RNA, and a non-functional protein might be produced. RNA therapies target these "mistakes" in the RNA so that a normal functional protein can be produced instead.
  • USH2A gene

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