A novel splice site mutation in the RDX gene causes DFNB24 hearing loss in an Iranian family

A. Eliot Shearer, Michael S. Hildebrand, Catherine J. Bromhead, Kimia Kahrizi, Jennifer A. Webster, Batool Azadeh, William J. Kimberling, Ali Anousheh, Arash Nazeri, Dietrich Stephan, Hossein Najmabadi, Richard J.H. Smith, Melanie Bahlo

Research output: Contribution to journalLetter

13 Scopus citations
Original languageEnglish (US)
Pages (from-to)555-558
Number of pages4
JournalAmerican Journal of Medical Genetics, Part A
Volume149
Issue number3
DOIs
StatePublished - Mar 1 2009

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

Shearer, A. E., Hildebrand, M. S., Bromhead, C. J., Kahrizi, K., Webster, J. A., Azadeh, B., Kimberling, W. J., Anousheh, A., Nazeri, A., Stephan, D., Najmabadi, H., Smith, R. J. H., & Bahlo, M. (2009). A novel splice site mutation in the RDX gene causes DFNB24 hearing loss in an Iranian family. American Journal of Medical Genetics, Part A, 149(3), 555-558. https://doi.org/10.1002/ajmg.a.32670