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., ...Daha Fazla

BMC MEDICAL GENETICS, cilt.16, 2015 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Özet

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