Ichthyosen
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Publisher
Springer Berlin Heidelberg
Link
http://link.springer.com/content/pdf/10.1007/978-3-642-24163-5_61
Reference25 articles.
1. Choate KA, Lu Y, Zhou J et al (2010) Mitotic recombination in patients with ichthyosis causes reversion of dominant mutations in KRT10. Science 330: 94–97
2. Eckl KM, de Juanes S, 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. 0J Invest Dermatol 129: 1421–1428
3. Elias PM, Williams ML, Holleran WM et al (2008) Pathogenesis of permeability barrier abnormalities in the ichthyoses: inherited disorders of lipid metabolism. J Lipid Res 49: 697–714
4. Elias P, Williams ML, Crumrine D, Schmuth M (2010) Ichthyoses - clinical, biochemical, pathogenic and diagnostic assessment, Vol 39. Karger, Basel
5. Fischer J (2009) Autosomal recessive congenital ichthyosis. J Invest Dermatol 129: 1319–1321
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Ichthyoses in everyday practice: management of a rare group of diseases;JDDG: Journal der Deutschen Dermatologischen Gesellschaft;2020-03
2. Ichthyosen im klinischen Alltag: Umgang mit einer seltenen Erkrankungsgruppe;JDDG: Journal der Deutschen Dermatologischen Gesellschaft;2020-03
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