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- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- Keratin gene mutations in disorders of human skin and its appendages
- A keratin scaffold regulates epidermal barrier formation, mitochondrial lipid composition, and activity
- Keratins and disease at a glance
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Molecular Genetics of Inherited Disorders of Epidermal Keratins
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