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Splice site and deletion mutations in keratin (KRT1 and KRT10) genes: unusual phenotypic alterations in Scandinavin patients with epidermolytic hyperkeratosis.
Uppsala University, Medicinska vetenskapsområdet, Faculty of Medicine, Department of Medical Sciences. (Dermatology and Venereology)
Uppsala University, Medicinska vetenskapsområdet, Faculty of Medicine, Department of Medical Sciences. (Dermatology and Venereology)
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2003 (English)In: J Invest Dermatol, Vol. 121, 1013- p.Article in journal (Refereed) Published
Place, publisher, year, edition, pages
2003. Vol. 121, 1013- p.
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URN: urn:nbn:se:uu:diva-65681OAI: oai:DiVA.org:uu-65681DiVA: diva2:93592
Available from: 2008-10-17 Created: 2008-10-17 Last updated: 2011-01-13

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