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A case of epidermolysis bullosa simplex with a newly found missense mutation and polymorphism in the highly conserved helix termination motif among type I keratins, which was previously reported as a pathogenic missense mutation



A case of epidermolysis bullosa simplex with a newly found missense mutation and polymorphism in the highly conserved helix termination motif among type I keratins, which was previously reported as a pathogenic missense mutation



British Journal of Dermatology 155(5): 1062-1063




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Accession: 048043541

Download citation: RISBibTeXText

PMID: 17034543

DOI: 10.1111/j.1365-2133.2006.07425.x


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