Prevalence and audiological profiles of GJB2 mutations in a large collective of hearing impaired patients-Reference-Cited by-同舟云学术

Prevalence and audiological profiles of GJB2 mutations in a large collective of hearing impaired patients

Published:2016-03 Issue: Volume:333 Page:77-86
ISSN:0378-5955
Container-title:Hearing Research
language:en
Short-container-title:Hearing Research

Author:

Burke W.F.^ORCID,Warnecke A.,Schöner-Heinisch A.,Lesinski-Schiedat A.,Maier H.,Lenarz T.

Publisher

Elsevier BV

Subject

Sensory Systems

Reference55 articles.

1. Frequency of congenital hearing loss in 43,503 healthy newborn infants in Konya, Turkey;Atas;JPMA – J. Pak. Med. Assoc.,2011

2. Ballana, E., Ventaol, M., Rabionet, R., Gasparini, P., Estivill, X., n.d. The Connexin-deafness Homepage [WWW Document]. Connexins Deaf. Homepage. URL http://www.crg.es/deafness (accessed 01.12.15.).

3. An overview of hereditary hearing loss;Bayazit;ORL,2006

4. Impaired permeability to Ins(1,4,5)P3 in a mutant connexin underlies recessive hereditary deafness;Beltramello;Nat. Cell Biol.,2005

5. The effects of violations of assumptions underlying the test;Boneau;Psychol. Bull.,1960

Cited by 17 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Preservation of developmental spontaneous activity enables early auditory system maturation in deaf mice;PLOS Biology;2023-06-27

2. Audiological Evidence of Frequent Hereditary Mild, Moderate and Moderate-to-Severe Hearing Loss;Journal of Personalized Medicine;2022-11-04

3. Preservation of prehearing spontaneous activity enables early auditory system development in deaf mice;2022-11-01

4. Extended genetic diagnostics for children with profound sensorineural hearing loss by implementing massive parallel sequencing. Diagnostic outcome, family experience and clinical implementation;International Journal of Pediatric Otorhinolaryngology;2022-08

5. Genetic etiology of non-syndromic hearing loss in Europe;Human Genetics;2022-01-19