Keratitis?ichthyosis?deafness syndrome: disease expression and spectrum of connexin 26 (GJB2) mutations in 14 patients-Reference-Cited by-同舟云学术

Keratitis?ichthyosis?deafness syndrome: disease expression and spectrum of connexin 26 (GJB2) mutations in 14 patients

Published:2007-05 Issue:5 Volume:156 Page:1015-1019
ISSN:0007-0963
Container-title:British Journal of Dermatology
language:en
Short-container-title:Br J Dermatol

Author:

Mazereeuw-Hautier J.,Bitoun E.,Chevrant-Breton J.,Man S.Y.K.,Bodemer C.,Prins C.,Antille C.,Saurat J.-H.,Atherton D.,Harper J.I.,Kelsell D.P.,Hovnanian A.

Publisher

Wiley

Subject

Dermatology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2133.2007.07806.x/fullpdf

Reference16 articles.

1. Keratitis, Ichthyosis, and Deafness (KID Syndrome): Review of the Literature and Proposal of a New Terminology

2. A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome

3. Missense Mutations in GJB2 Encoding Connexin-26 Cause the Ectodermal Dysplasia Keratitis-Ichthyosis-Deafness Syndrome

4. GJB2mutations in keratitis-ichthyosis-deafness syndrome including its fatal form

5. HID and KID syndromes are associated with the same connexin 26 mutation

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