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Original article
Prevalence of mitochondrial DNA mutations in childhood/congenital onset non-syndromal sensorineural hearing impairment
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Authors

  1. Dr Hutchin,t.p.hutchin{at}leeds.ac.uk
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Citation

Hutchin TP, Thompson KR, Parker M, et al
Prevalence of mitochondrial DNA mutations in childhood/congenital onset non-syndromal sensorineural hearing impairment
Journal of Medical Genetics 2001;38:229-231.

Publication history

  • Revised January 25, 2001
  • Accepted January 30, 2001
  • First published April 1, 2001.
Online issue publication 
April 01, 2001

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Journal of Medical Genetics