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...

Descripción completa

Detalles Bibliográficos
Autores principales: Chao, Xiuhua, Xiao, Yun, Zhang, Fengguo, Luo, Jianfen, Wang, Ruijie, Liu, Wenwen, Wang, Haibo, Xu, Lei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7481964/
https://www.ncbi.nlm.nih.gov/pubmed/32952548
http://dx.doi.org/10.1155/2020/8829587

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7481964/
https://www.ncbi.nlm.nih.gov/pubmed/32952548
http://dx.doi.org/10.1155/2020/8829587

Ejemplares similares