Progressive symmetrical erythrokeratoderma: report of two Chinese families and evaluation for mutations in the loricrin, connexin 30.3 and connexin 31 genes

Clin Exp Dermatol. 2013 Dec;38(8):925-7. doi: 10.1111/ced.12135. Epub 2013 May 17.

Authors

B-R Guo¹, L-D Sun, Y Cui, S Yang, X-J Zhang

Affiliation

¹ Institute and Department of Dermatology, No. 1 Hospital, Anhui Medical University, Hefei, Anhui, China; State Key Laboratory Incubation Base of Dermatology, Ministry of National Science and Technology, Hefei, Anhui, China.

PMID: 23678955
DOI: 10.1111/ced.12135

No abstract available

Publication types

Case Reports
Letter
Research Support, Non-U.S. Gov't

MeSH terms

Adolescent
Adult
Asian People / genetics
China
Connexins / genetics*
Erythema / genetics*
Female
Humans
Keratosis / genetics*
Male
Membrane Proteins / genetics*
Mutation*

Substances

Connexins
Membrane Proteins
loricrin
GJB3 protein, human
connexin 30.3