Connexin 26 gene linked to a dominant deafness (Q47991729)

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scientific article published in May 1998

Language	Label	Description	Also known as
English	Connexin 26 gene linked to a dominant deafness	scientific article published in May 1998

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/9620796

Connexin 26 gene linked to a dominant deafness (English)

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/9620796

1 reference

based on heuristic

inferred from title

Christine Petit

8

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/9620796

author name string

F Denoyelle

1

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/9620796

G Lina-Granade

2

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/9620796

H Plauchu

3

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/9620796

R Bruzzone

4

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/9620796

H Chaïb

5

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/9620796

F Lévi-Acobas

6

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/9620796

D Weil

7

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/9620796

language of work or name

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publication date

1 May 1998

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/9620796

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/9620796

393

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/9620796

6683

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/9620796

319-320

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/9620796

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

1 reference

https://api.crossref.org/works/10.1038%2F30639

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2F30639

21 January 2018

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/10.1038%2F30639

21 January 2018

Connexin mutations and hearing loss

1 reference

https://api.crossref.org/works/10.1038%2F30639

21 January 2018

Genes responsible for human hereditary deafness: symphony of a thousand

1 reference

https://api.crossref.org/works/10.1038%2F30639

21 January 2018

The cellular Internet: on-line with connexins

1 reference

https://api.crossref.org/works/10.1038%2F30639

21 January 2018

Mutational analysis of gap junction formation

1 reference

https://api.crossref.org/works/10.1038%2F30639

21 January 2018

Structure of gap junction intercellular channels

1 reference

https://api.crossref.org/works/10.1038%2F30639

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2F30639

21 January 2018

The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene

1 reference

https://api.crossref.org/works/10.1038%2F30639

21 January 2018

Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene

1 reference

https://api.crossref.org/works/10.1038%2F30639

21 January 2018

A gene responsible for a dominant form of neurosensory non-syndromic deafness maps to the NSRD1 recessive deafness gene interval

1 reference

https://api.crossref.org/works/10.1038%2F30639

21 January 2018

Identifiers

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/9620796

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/9620796

ResearchGate publication ID

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