Mutations of KRT6A are more frequent than those of KRT16 in pachyonychia congenita type 1: report of a novel and a recently reported mutation in two unrelated Chinese families-Reference-Cited by-同舟云学术

Mutations of KRT6A are more frequent than those of KRT16 in pachyonychia congenita type 1: report of a novel and a recently reported mutation in two unrelated Chinese families

Published:2008-07 Issue:1 Volume:159 Page:238-240
ISSN:0007-0963
Container-title:British Journal of Dermatology
language:en
Short-container-title:Br J Dermatol

Author:

Bai Z-L.,Feng Y-G.,Tan S-S.,Wang X-Y.,Xiao S-X.,Wang H.,Jia H-Q.,Wu J-W.,He D-L.,Kang R-H.

Publisher

Wiley

Subject

Dermatology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2133.2008.08603.x/fullpdf

Reference9 articles.

1. Human keratin diseases: the increasing spectrum of disease and subtlety of the phenotype-genotype correlation

2. The molecular genetics of the genodermatoses: progress to date and future directions

3. A current and online genodermatosis database

4. Novel proline substitution mutations in keratin 16 in two cases of pachyonychia congenita type 1

5. A mutation detection strategy for the human keratin 6A gene and novel missense mutations in two cases of pachyonychia congenita type 1

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