Connecting with connexins-Reference-Cited by-同舟云学术

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Connecting with connexins

Published:2013-06-28 Issue:4 Volume:54 Page:287-289
ISSN:0004-8380
Container-title:Australasian Journal of Dermatology
language:en
Short-container-title:Australasian Journal of Dermatology

Author:

Williams Penelope¹,Memon Aamir²,Sinha Tapati²,Fryer Alan³

Affiliation:

1. Department of Dermatology; Royal Liverpool and Broadgreen Hospital NHS Trust; Southport UK

2. Department of Dermatology; Southport and Ormskirk Hospital NHS Trust; Southport UK

3. Alder Hey Children's NHS Foundation Trust and Liverpool Women's NHS Foundation Trust; Southport UK

Publisher

Wiley

Subject

Dermatology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/ajd.12070/fullpdf

Reference12 articles.

1. Connexins, connexons, and intercellular communication;Goodenough;Annu. Rev. Biochem.,1996

2. Gap junction diseases of the skin;Steensel;Am. J. Med. Genet. C Semin. Med. Genet.,2004

3. Clinical phenotype and mutations in connexin 26 (DFNB1/GJB2), the most common cause of childhood hearing loss;Cohn;Am. J. Med. Genet.,1999

4. A connexin 26 mutation causes a syndrome of sensorineural hearing loss and palmoplantar hyperkeratosis;Heathcote;J. Med. Genet.,2000

5. Mutations in GJB-2 encoding connexin- 26 cause the ectodermal dysplasia keratitis-ichthyosis-deafness syndrome;Richard;Am. J. Hum. Genet.,2002

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