Interactions of genetic variations in FAS, GJB2 and PTPRN2 are associated with noise-induced hearing loss: a case-control study in China
Abstract Background This study aimed to screen and validate noise-induced hearing loss (NIHL) associated single nucleotide polymorphisms (SNPs), construct genetic risk prediction models, and evaluate higher-order gene-gene, gene-environment interactions for NIHL in Chinese population. Methods First,...
Saved in:
Main Authors: | Shan Wu (Author), Zhidan Wu (Author), Manlian Chen (Author), Xiangbin Zhong (Author), Haoyan Gu (Author), Wenjing Du (Author), Weidong Liu (Author), Li Lang (Author), Junyi Wang (Author) |
---|---|
Format: | Book |
Published: |
BMC,
2024-01-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Screening of Autosomal Recessive Non-Syndromic Hearing Loss gor GJB2 Mutations
by: Atefeh Khosh-Aeen, et al.
Published: (2004) -
Volumetric Analysis of Hearing-Related Structures of Brain in Children with GJB2-Related Congenital Deafness
by: Matthias W. Wagner, et al.
Published: (2022) -
TONAL AUDIOLOGICAL PERFORMANCE EVALUATION AFTER COCHLEAR IMPLANTATION IN CHILDREN WITH GJB2 GENE RELATED HEARING LOSS
by: Martu Cristian, et al.
Published: (2011) -
Genetic Linkage Analysis of DFNB4, DFNB28, DFNB93 Loci in Autosomal Recessive Non-syndromic Hearing Loss: Evidence for Digenic Inheritance in GJB2 and GJB3 Mutations
by: Marzieh NASERI, et al.
Published: (2017) -
Associations of noise kurtosis, genetic variations in NOX3 and lifestyle factors with noise-induced hearing loss
by: Tianyu Zhao, et al.
Published: (2020)