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

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