Keratin 17 mutation in pachyonychia congenita type 2 with early onset sebaceous cysts
Author:
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2133.2003.05152.x/fullpdf
Reference22 articles.
1. Do the ends justify the mean? Proline mutations at the ends of the keratin coiled-coil rod segment are more disruptive than internal mutations.
2. Keratin diseases
3. Human keratin diseases:. Hereditary fragility of specific epithelial tissues
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