Novel domain-specific POU3F4 mutations are associated with X-linked deafness: examples from different populations

Bademci G., Lasisi A. O., Yariz K. O., Montenegro P., Menendez I., Vinueza R., ...More

BMC MEDICAL GENETICS, vol.16, 2015 (SCI-Expanded, Scopus)

  • Publication Type: Article / Article
  • Volume: 16
  • Publication Date: 2015
  • Doi Number: 10.1186/s12881-015-0149-2
  • Journal Name: BMC MEDICAL GENETICS
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Hacettepe University Affiliated: Yes

Abstract

Background: Mutations in the POU3F4 gene cause X-linked deafness type 3 (DFN3), which is characterized by inner ear anomalies.