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

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

BMC medical genetics, cilt.16, ss.9, 2015 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 16
  • Basım Tarihi: 2015
  • Doi Numarası: 10.1186/s12881-015-0149-2
  • Dergi Adı: BMC medical genetics
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.9
  • Eskişehir Osmangazi Üniversitesi Adresli: Evet

Özet

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