(Q50489151)

14 March 2018

title

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

1 reference

14 March 2018

1

B Engel-Yeger

2 references

ORCID Public Data File 2021

14 March 2018

author name string

S Zaaroura

2

1 reference

14 March 2018

J Zlotogora

3

1 reference

14 March 2018

S Shalev

4

1 reference

14 March 2018

Y Hujeirat

5

1 reference

14 March 2018

M Carrasquillo

6

1 reference

14 March 2018

S Barges

7

1 reference

14 March 2018

H Pratt

8

1 reference

14 March 2018

publication date

1 January 2002

1 reference

14 March 2018

published in

Hearing Research

1 reference

14 March 2018

volume

163

1 reference

14 March 2018

issue

1-2

1 reference

14 March 2018

page(s)

93-100

1 reference

14 March 2018

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

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2801%2900386-0

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%2801%2900386-0

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%2801%2900386-0

7 January 2021

Connexin 26 gene linked to a dominant deafness

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2801%2900386-0

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%2801%2900386-0

7 January 2021

Connexin-26 mutations in sporadic and inherited sensorineural deafness

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2801%2900386-0

7 January 2021

Transplacental uptake of glucose is decreased in embryonic lethal connexin26-deficient mice

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2801%2900386-0

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2801%2900386-0

7 January 2021

Connexin 26: required for normal auditory function

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2801%2900386-0

7 January 2021

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2801%2900386-0

7 January 2021

Gap junctions in the rat cochlea: immunohistochemical and ultrastructural analysis

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2801%2900386-0

7 January 2021

Gap junction systems in the mammalian cochlea

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2801%2900386-0

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%2801%2900386-0

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%2801%2900386-0

7 January 2021

Connexin-26 mutations in sporadic non-syndromal sensorineural deafness

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2801%2900386-0

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%2801%2900386-0

7 January 2021

Relation between choice of partner and high frequency of connexin-26 deafness

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2801%2900386-0

7 January 2021

Molecular genetics applied to clinical practice: the Cx26 hearing impairment.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2801%2900386-0

7 January 2021

Connexin26 mutations associated with nonsyndromic hearing loss.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2801%2900386-0

7 January 2021

Connexin 26 gene mutation and autosomal recessive deafness

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2801%2900386-0

7 January 2021

10.1016/S0378-5955(01)00386-0

Identifiers

DOI

1 reference

14 March 2018

1 reference

14 March 2018