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Neural Plasticity
Volume 2016, Article ID 1512831, 10 pages
Research Article

A Novel Nonsense Mutation of POU4F3 Gene Causes Autosomal Dominant Hearing Loss

1Department of Otorhinolaryngology Head and Neck Surgery, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, China
2Shandong Provincial Key Laboratory of Otology, Jinan, China
3Department of Otolaryngology-Head & Neck Surgery, Case Western Reserve University, Cleveland, OH, USA

Received 18 July 2016; Revised 11 October 2016; Accepted 24 October 2016

Academic Editor: Genglin Li

Copyright © 2016 Chi Zhang et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Supplementary Material

Summary of 81 Genes related to non-syndromic hearing loss in target region capture sequencing. Name, inheritance pattern, GenBank accession number and exon count of each gene are shown in the table. AR: Autosomal Recessive; AD: Autosomal Dominant; MT: Mitochondrial Inheritance.

  1. Supplementary Material