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palmoplantar keratoderma, nonepidermolytic
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KRT1
PKC epsilon is associated with myosin IIA and actin in fibroblasts
New mutations in keratin 1 that cause bullous congenital ichthyosiform erythroderma and keratin 2e that cause ichthyosis bullosa of Siemens
Keratins of the human hair follicle
KRT16
Novel mutations in keratin 16 gene underlie focal non-epidermolytic palmoplantar keratoderma (NEPPK) in two families
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wnt signaling pathway
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{:one=>"one gene", :other=>"%{count} genes"}
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