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  • Clinical and molecular genetic characterisation of a family segregating autosomal dominant retinitis pigmentosa and sensorineural deafness

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Original Article
Clinical and molecular genetic characterisation of a family segregating autosomal dominant retinitis pigmentosa and sensorineural deafness

Authors

  1. Paul F Kenna, Wellcome Ocular Genetics Unit, Biotechnology Institute, Trinity College, Lincoln Gate, Dublin 2, Ireland.
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Citation

Kenna P, Mansergh F, Millington-Ward S, et al
Clinical and molecular genetic characterisation of a family segregating autosomal dominant retinitis pigmentosa and sensorineural deafness
British Journal of Ophthalmology 1997;81:207-213.

Publication history

  • Accepted November 15, 1996
  • First published March 1, 1997.
Online issue publication 
January 23, 2023

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Copyright information

British Journal of Ophthalmology