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BioMed Research International
Volume 2017 (2017), Article ID 4707315, 8 pages
https://doi.org/10.1155/2017/4707315
Research Article

Novel Mutations and Mutation Combinations of TMPRSS3 Cause Various Phenotypes in One Chinese Family with Autosomal Recessive Hearing Impairment

1Department of Otolaryngology, The General Hospital of the PLA Rocket Force, No. 16 Xinwai Dajie, Beijing 100088, China
2Department of Otolaryngology, Head and Neck Surgery, PLA General Hospital, No. 28 Fuxing Road, Beijing 100853, China
3Department of Otolaryngology, Emory University School of Medicine, 615 Michael Street, Whitehead Biomedical Research Bldg, Rm No. 543, Atlanta, GA 30322, USA

Correspondence should be addressed to Xi Lin; ude.yrome@2nilx and Pu Dai; moc.anis.piv@103upiad

Received 12 October 2016; Revised 3 December 2016; Accepted 20 December 2016; Published 29 January 2017

Academic Editor: Jozef Anné

Copyright © 2017 Xue Gao 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

129 deafness genes list includes the information of NCBI Reference, OMIM, Description, CDS bps, # of Exons, Covered Region, inheritance pattern and syndromic or not

  1. Supplementary Material