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., ...More

BMC medical genetics, vol.16, pp.9, 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
• Page Numbers: pp.9
• Open Archive Collection: AVESIS Open Access Collection
• Eskisehir Osmangazi University Affiliated: Yes

Abstract

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