(Q28117673)

4 January 2017

title

Connexin-26 mutations in sporadic and inherited sensorineural deafness (English)

1 reference

4 January 2017

1 reference

R. Rabionet

4

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Montserrat Milà

object named as

M. Milà

Xavier Estivill i Pallejà

10

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object named as

X. Estivill

1

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author name string

P. Fortina

2

1 reference

4 January 2017

S. Surrey

3

1 reference

4 January 2017

S. Melchionda

5

1 reference

4 January 2017

L. D'Agruma

6

1 reference

4 January 2017

E. Mansfield

7

1 reference

4 January 2017

E. Rappaport

8

1 reference

4 January 2017

N. Govea

9

1 reference

4 January 2017

L. Zelante

11

1 reference

4 January 2017

P. Gasparini

12

1 reference

4 January 2017

language of work or name

English

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publication date

7 February 1998

1 reference

4 January 2017

1 reference

4 January 2017

volume

351

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4 January 2017

issue

9100

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4 January 2017

page(s)

394–398

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2911124-2

4 January 2017

1 reference

7 January 2021

Genes responsible for human hereditary deafness: symphony of a thousand

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2911124-2

7 January 2021

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2911124-2

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%2FS0140-6736%2897%2911124-2

7 January 2021

Mutations in the myosin VIIA gene cause non-syndromic recessive deafness

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2911124-2

7 January 2021

Defective myosin VIIA gene responsible for Usher syndrome type 1B

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2911124-2

7 January 2021

Nonsyndromic deafness DFNA1 associated with mutation of a human homolog of the Drosophila gene diaphanous

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2911124-2

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%2FS0140-6736%2897%2911124-2

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%2FS0140-6736%2897%2911124-2

7 January 2021

Assignment of connexin 26 (GJB2) and 46 (GJA3) genes to human chromosome 13q11-->q12 and mouse chromosome 14D1-E1 by in situ hybridization

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2911124-2

7 January 2021

Connexin family of gap junction proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2911124-2

7 January 2021

Structure--function relationships in gap junctions.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2911124-2

7 January 2021

Synaptic transmission: a bidirectional and self-modifiable form of cell-cell communication

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2911124-2

7 January 2021

Tight and gap junctions in a vertebrate inner ear

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2911124-2

7 January 2021

Receptor synapses without synaptic ribbons in the cochlea of the cat

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2911124-2

7 January 2021

Gap junctions in the rat cochlea: immunohistochemical and ultrastructural analysis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2911124-2

7 January 2021

Changes in immunostaining of cochleas with experimentally induced endolymphatic hydrops

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2911124-2

7 January 2021

Mixing of connexins in gap junction membrane channels

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2911124-2

7 January 2021

Connexin mutations in X-linked Charcot-Marie-Tooth disease

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2911124-2

7 January 2021

10.1016/S0140-6736(97)11124-2

Identifiers

DOI

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017