Progressive symmetrical erythrokeratoderma: report of a Turkish family and evaluation for loricrin and connexin gene mutations
Author:
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2230.2008.02728.x/fullpdf
Reference10 articles.
1. Erythrokeratodermia progressiva symmetrica. Report of 10 cases;Ruiz-Maldonado;Dermatologica,1982
2. Progressive symmetric erythrokeratodermia;Gray;J Am Acad Dermatol,1996
3. Connexin disorders of the skin;Richard;Clin Dermatol,2005
4. The molecular pathology of progressive symmetric erythrokeratoderma: a frameshift mutation in the loricrin gene and perturbations in the cornified cell envelope;Ishida-Yamamoto;Am J Hum Gene,1997
5. Identification of a novel locus for progressive symmetric erythrokeratodermia to a 19.02-cM Interval at 21q11.2-21q21.2;Chui;J Invest Dermatol,2006
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