Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2
Author:
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2133.1998.02413.x/fullpdf
Reference28 articles.
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3. Do the ends justify the means? Proline mutations at the ends of the keratin coiled-coil rod segment are more disruptive than internal mutations;Letai;J Cell Biol,1992
4. Keratin intermediate filament structure: crosslinking studies yield quantitative information on molecular dimensions and mechanism of assembly;Steinert;J Mol Biol,1993
5. Concurrence between the molecular overlap regions in keratin intermediate filaments and the locations of keratin mutations in genodermatoses;Steinert;Biochem Biophys Res Commun,1993
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