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A novel mutation in the mitochondrial tRNASer(UCN) gene in a family with non-syndromic sensorineural hearing impairment
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Authors

  1. Dr Hutchin, Molecular Medicine Unit, Clinical Sciences Building, St James's University Hospital, Beckett Street, Leeds LS9 7TF, UK,t.p.hutchin{at}leeds.ac.uk
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Citation

Hutchin TP, Parker MJ, Young ID, et al
A novel mutation in the mitochondrial tRNASer(UCN) gene in a family with non-syndromic sensorineural hearing impairment
Journal of Medical Genetics 2000;37:692-694.

Publication history

  • Revised March 22, 2000
  • Accepted April 10, 2000
  • First published September 1, 2000.
Online issue publication 
September 01, 2000

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Journal of Medical Genetics