An asparagine to threonine substitution in the 1A domain of keratin 1: a novel mutation that causes epidermolytic hyperkeratosis
Author:
Publisher
Wiley
Subject
Dermatology,Molecular Biology,Biochemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0625.1999.tb00359.x/fullpdf
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1. Pair formation and promiscuity of cytokeratins: formation in vitro of heterotypic complexes and intermediate-sized filaments by homologous and heterologous recombinations of purified polypeptides.
2. Defects in the Barrier
3. Mutations in the Rod Domains of Keratins 1 and 10 in Epidermolytic Hyperkeratosis
4. The genetic basis of epidermolytic hyperkeratosis: A disorder of differentiation-specific epidermal keratin genes
5. A leucine→proline mutation in the H1 subdomain of keratin 1 causes epidermolytic hyperkeratosis
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