Sökning: "EHK"
Hittade 1 avhandling innehållade ordet EHK.
1. On keratin mutations in epidermolytic hyperkeratosis and the regulation of keratin expression by retinoids
Sammanfattning : Epidermolytic hyperkeratosis is a rare inherited disease of the skin caused by a dominant-negative mutation in keratin 1 (K1) or 10 (K10). Keratins are the major structural protein in epidermis and mutations causes instability of intermediate filament and keratinocyte fragility. LÄS MER
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