Prevalence and Characteristics of STRC Gene Mutations (DFNB16): A Systematic Review and Meta-Analysis

Prevalence and Characteristics of STRC Gene Mutations (DFNB16): A Systematic Review and Meta-Analysis

Background: Mutations in the STRC (MIM 606440) gene, inducing DFNB16, are considered a major cause of mild–moderate autosomal recessive non-syndromic hearing loss (ARNSHL). We conducted a systematic review and meta-analysis to determine the global prevalence and characteristics of STRC variations, i...

Full description

Bibliographic Details
Main Authors: Shuang Han, Dejun Zhang, Yingyuan Guo, Zeming Fu, Guofang Guan
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-09-01
Series:Frontiers in Genetics
Subjects:
STRC gene
mutation
deafness
prevalence
meta-analysis
Online Access:https://www.frontiersin.org/articles/10.3389/fgene.2021.707845/full

Similar Items

Similar Items