Klinik und Ätiologie der Ichthyosen
Author:
Publisher
Springer Science and Business Media LLC
Subject
Dermatology
Link
http://link.springer.com/content/pdf/10.1007/s00105-010-2018-4.pdf
Reference20 articles.
1. Eckl KM, de JS, Kurtenbach J et al (2009) Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: Evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12B. J Invest Dermatol 129(6):1421–1428
2. Elias PM, Williams ML, Holleran WM et al (2008) Thematic review series: skin lipids. Pathogenesis of permeability barrier abnormalities in the ichthyoses: inherited disorders of lipid metabolism. J Lipid Res 49:697–714
3. Dahlqvist J, Klar J, Tiwari N et al (2010) A single-nucleotide deletion in the POMP 5‘ UTR causes a transcriptional switch and altered epidermal proteasome distribution in KLICK genodermatosis. Am J Hum Genet 86:596–603
4. Fischer J (2009) Autosomal recessive congenital ichthyosis. J Invest Dermatol 129:1319–1321
5. Frost P, Weinstein GD, Van Scott EJ (1966) The ichthyosiform dermatoses. II. Autoradiographic studies of epidermal proliferation. J Invest Dermatol 47:561–567
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