A recurrent mutation in the TGM5 gene in European patients with acral peeling skin syndrome

Bibliographic Details

Published in:	Journal of dermatological science 2012-01, Vol.65 (1), p.74-76
Main Authors:	van der Velden, J.J.A.J, Jonkman, M.F, McLean, W.H.I, Hamm, H, Steijlen, P.M, van Steensel, M.A.M, van Geel, M
Format:	Article
Language:	eng
Subjects:	Acral peeling skin syndrome Bullous disease Dermatitis, Exfoliative - genetics Dermatology DNA Mutational Analysis Europe Family Health Founder mutation Genetics Haplotypes Haplotyping analysis Homozygote Humans Models, Genetic Mutation Pigmentation Disorders - genetics Skin Diseases - congenital Skin Diseases, Vesiculobullous - genetics Transglutaminases - genetics
Online Access:	Get full text
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