(Q48409901)

11 February 2018

title

Otoacoustic emissions and brainstem evoked potentials in compound carriers of connexin 26 mutations. (English)

1 reference

11 February 2018

1

B Engel-Yeger

2 references

ORCID Public Data File 2021

11 February 2018

author name string

S Zaaroura

2

1 reference

11 February 2018

J Zlotogora

3

1 reference

11 February 2018

S Shalev

4

1 reference

11 February 2018

Y Hujeirat

5

1 reference

11 February 2018

M Carrasquillo

6

1 reference

11 February 2018

B Saleh

7

1 reference

11 February 2018

H Pratt

8

1 reference

11 February 2018

publication date

1 January 2003

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11 February 2018

published in

Hearing Research

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11 February 2018

volume

175

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11 February 2018

issue

1-2

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11 February 2018

page(s)

140-151

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11 February 2018

Prevalent connexin 26 gene (GJB2) mutations in Japanese

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900719-0

7 January 2021

Connections with connexins: the molecular basis of direct intercellular signaling

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900719-0

7 January 2021

Two different connexin 26 mutations in an inbred kindred segregating non-syndromic recessive deafness: implications for genetic studies in isolated populations.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900719-0

7 January 2021

Clinical studies of families with hearing loss attributable to mutations in the connexin 26 gene (GJB2/DFNB1)

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900719-0

7 January 2021

Clinical features of the prevalent form of childhood deafness, DFNB1, due to a connexin-26 gene defect: implications for genetic counselling.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900719-0

7 January 2021

Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900719-0

7 January 2021

The effects of a connexin 26 mutation--35delG--on oto-acoustic emissions and brainstem evoked potentials: homozygotes and carriers.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900719-0

7 January 2021

Connexin-26 mutations in sporadic and inherited sensorineural deafness

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900719-0

7 January 2021

Epidemiology of permanent childhood hearing impairment in Trent Region, 1985-1993.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900719-0

7 January 2021

Connexins, connexons, and intercellular communication

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900719-0

7 January 2021

Autosomal recessive nonsyndromic neurosensory deafness at DFNB1 not associated with the compound-heterozygous GJB2 (connexin 26) genotype M34T/167delT.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900719-0

7 January 2021

Connexin 26: required for normal auditory function

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900719-0

7 January 2021

Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNB1) hearing loss

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900719-0

7 January 2021

Gap junctions in the rat cochlea: immunohistochemical and ultrastructural analysis

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900719-0

7 January 2021

Gap junction systems in the mammalian cochlea

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900719-0

7 January 2021

Novel mutations in the connexin 26 gene (GJB2) responsible for childhood deafness in the Japanese population.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900719-0

7 January 2021

Expression of the gap-junction connexins 26 and 30 in the rat cochlea

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900719-0

7 January 2021

Connexins, hearing and deafness: clinical aspects of mutations in the connexin 26 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900719-0

7 January 2021

Properties of connexin26 gap junctional proteins derived from mutations associated with non-syndromal heriditary deafness

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900719-0

7 January 2021

Mutations in the connexin 26 gene (GJB2) among Ashkenazi Jews with nonsyndromic recessive deafness

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900719-0

7 January 2021

Genetic epidemiology of hearing impairment

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900719-0

7 January 2021

Connexin26 mutations associated with nonsyndromic hearing loss.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900719-0

7 January 2021

New functions for gap junctions

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900719-0

7 January 2021

At the speed of sound: gene discovery in the auditory system

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900719-0

7 January 2021

A common founder for the 35delG GJB2 gene mutation in connexin 26 hearing impairment.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900719-0

7 January 2021

High frequency hearing loss correlated with mutations in the GJB2 gene.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900719-0

7 January 2021

Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900719-0

7 January 2021

10.1016/S0378-5955(02)00719-0

Identifiers

DOI

1 reference

11 February 2018

release_jklexyh2pjcollxdo6uwafrwya

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/jklexyh2pjcollxdo6uwafrwya

24 November 2022

mapped directly with Wikidata item

1 reference

11 February 2018