Cochlear Implantation in a Patient with a Novel POU3F4 Mutation and Incomplete Partition Type-III Malformation

Aims. This study is aimed at (1) analyzing the clinical manifestations and genetic features of a novel POU3F4 mutation in a nonsyndromic X-linked recessive hearing loss family and (2) reporting the outcomes of cochlear implantation in a patient with this mutation. Methods. A patient who was diagnose...

Full description

Bibliographic Details
Main Authors: Xiuhua Chao, Yun Xiao, Fengguo Zhang, Jianfen Luo, Ruijie Wang, Wenwen Liu, Haibo Wang, Lei Xu
Format: Article
Language:English
Published: Hindawi Limited 2020-01-01
Series:Neural Plasticity
Online Access:http://dx.doi.org/10.1155/2020/8829587