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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...

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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

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