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Low prevalence of DFNB1 (connexin 26) mutations in British Pakistani children with non-syndromic sensorineural hearing loss
  1. Soo Y Yoong1,
  2. Lampros A Mavrogiannis2,
  3. John Wright3,
  4. Lesley Fairley3,
  5. Christopher P Bennett4,
  6. Ruth S Charlton2,
  7. Nick Spencer5
  1. 1Community Paediatrics, St Luke's Hospital, Bradford, UK
  2. 2DNA Laboratory, Yorkshire Regional Genetics Service, St James's University Hospital, Leeds, UK
  3. 3Bradford Institute for Health Research, Bradford Royal Infirmary, Bradford, UK
  4. 4Clinical Genetics, Yorkshire Regional Genetics Service, St James's University Hospital, Leeds, UK
  5. 5School of Health and Social Studies, University of Warwick, Coventry, UK
  1. Correspondence to Dr Soo Y Yoong, St Luke's Hospital, Little Horton Lane, Bradford BD5 0NA, UK; soo.yoong{at}bradfordhospitals.nhs.uk

Footnotes

  • Competing interests None.

  • Provenance and peer review Not commissioned; externally peer reviewed.

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Footnotes

  • Competing interests None.

  • Provenance and peer review Not commissioned; externally peer reviewed.

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