Mutation analysis of common deafness genes among 1,201 patients with non‐syndromic hearing loss in S...
Mutation analysis of common deafness genes among 1,201 patients with non‐syndromic hearing loss in Shanxi Province
About this item
Full title
Author / Creator
Zhou, Yongan , Li, Chao , Li, Min , Zhao, Zhonghua , Tian, Shuxiong , Xia, Hou , Liu, Peixian , Han, Yaxin , Ren, Ruirui , Chen, Jianping , Jia, Caihong and Guo, Wei
Publisher
United States: John Wiley & Sons, Inc
Journal title
Language
English
Formats
Publication information
Publisher
United States: John Wiley & Sons, Inc
Subjects
More information
Scope and Contents
Contents
Background
Hearing impairment is one of most frequent birth defects, which affects nearly 1 in every 1,000 live births. However, the molecular etiology of non‐syndromic deafness in China is not well studied. Here, we have investigated the presence of mutations in three genes commonly mutated in non‐syndromic deafness patients in Shanxi Province,...
Alternative Titles
Full title
Mutation analysis of common deafness genes among 1,201 patients with non‐syndromic hearing loss in Shanxi Province
Authors, Artists and Contributors
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6418354
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6418354
Other Identifiers
ISSN
2324-9269
E-ISSN
2324-9269
DOI
10.1002/mgg3.537
