(Q28204619)

2

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X Chen

3

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N Ohtake

4

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A Tomitaka

5

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H Akamatsu

6

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K Matsunaga

7

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S Shiraishi

8

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H Miura

9

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J Adachi

10

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T Kanzaki

British Journal of Dermatology

11

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language of work or name

English

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publication date

April 2003

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published in

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volume

148

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issue

4

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page(s)

649-53

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cites work

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

1 reference

https://api.crossref.org/works/10.1046/J.1365-2133.2003.05245.X

A Congenital Ichthyosiform Syndrome With Deafness and Keratitis

21 April 2017

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2133.2003.05245.X

Functional defects of Cx26 resulting from a heterozygous missense mutation in a family with dominant deaf-mutism and palmoplantar keratoderma.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2133.2003.05245.X

A connexin 26 mutation causes a syndrome of sensorineural hearing loss and palmoplantar hyperkeratosis (MIM 148350)

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2133.2003.05245.X

A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated families

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2133.2003.05245.X

Connexin mutations in skin disease and hearing loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2133.2003.05245.X

A novel connexin 26 mutation in a patient diagnosed with keratitis-ichthyosis-deafness syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2133.2003.05245.X

Missense mutations in GJB2 encoding connexin-26 cause the ectodermal dysplasia keratitis-ichthyosis-deafness syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2133.2003.05245.X

Connections with connexins: the molecular basis of direct intercellular signaling

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2133.2003.05245.X

Genetic diseases and gene knockouts reveal diverse connexin functions.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2133.2003.05245.X

Connexins: a connection with the skin

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2133.2003.05245.X

Keratitis, ichthyosis, and deafness (KID) syndrome. Vertical transmission and death from multiple squamous cell carcinomas

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2133.2003.05245.X

Functional analysis of human Cx26 mutations associated with deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2133.2003.05245.X

10.1046/J.1365-2133.2003.05245.X

21 January 2018

Identifiers

DOI

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

12752120

1 reference

Consolidated OpenCitations Corpus – April 2017