A novel mutation in a family with non-syndromic sensorineural hearing loss that disrupts the newly characterised OTOF long isoforms.

M. J. Houseman, A. P. Jackson, L. I. Al-Gazali, R. A. Badin, E. Roberts, R. F. Mueller

Research output: Contribution to journalLetterpeer-review

33 Citations (Scopus)
Original languageEnglish
Pages (from-to)E25
JournalJournal of medical genetics
Issue number8
Publication statusPublished - Aug 2001
Externally publishedYes

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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