Clinical heterogeneity in recessive epidermolysis bullosa due to mutations in the keratin 14 gene,KRT14
Author:
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2230.2008.02858.x/fullpdf
Reference24 articles.
1. Progress in epidermolysis bullosa: from eponyms to molecular genetic classification;Uitto;Clin Dermatol,2005
2. A comparative study between transmission electron microscopy and immunofluorescence mapping in the diagnosis of epidermolysis bullosa;Yiasemides;Am J Dermatopathol,2006
3. Partial revertant mosaicism of keratin 14 in a patient with recessive epidermolysis bullosa simplex;Schuilenga-Hut;J Invest Dermatol,2002
4. Genomic organization and amplification of the human epidermal type II keratin genes K1 and K5;Whittock;Biochem Biophys Res Comms,2000
5. Dominant and recessive compound heterozygous mutations in epidermolysis bullosa simplex demonstrate the role of the stutter region in keratin intermediate filament assembly;Yasukawa;J Biol Chem,2002
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