Literature DB >> 21777220

A novel mutation in CDSN causes peeling skin disease in a patient from Morocco.

J Mazereeuw-Hautier, E A Leclerc, M Simon, G Serre, N Jonca.   

Abstract

Entities:  

Mesh：

Substances：

Year:  2011        PMID： 21777220     DOI： 10.1111/j.1365-2133.2011.10529.x

Source DB:  PubMed          Journal:  Br J Dermatol        ISSN： 0007-0963            Impact factor:   9.302


× No keyword cloud information.
  3 in total

Review 1.  Epidermal barrier disorders and corneodesmosome defects.

Authors:  Marek Haftek
Journal:  Cell Tissue Res       Date:  2014-11-07       Impact factor: 5.249

2.  A Case of Inflammatory Generalized Type of Peeling Skin Syndrome Possibly Caused by a Homozygous Missense Mutation of CDSN.

Authors:  Hiroshi Kawakami; Masaki Uchiyama; Tatsuo Maeda; Takahiko Tsunoda; Yoshihiko Mitsuhashi; Ryoji Tsuboi
Journal:  Case Rep Dermatol       Date:  2014-10-11

3.  A novel pathogenic variant in the corneodesmosin gene causing generalized inflammatory peeling skin syndrome with marked eosinophilia and trichorrhexis invaginata.

Authors:  Helen Gordon; Patrick Yap; Kuang-Chih Hsiao; Michael Watson; Diana Purvis
Journal:  Pediatr Dermatol       Date:  2022-02-17       Impact factor: 1.997
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.