Tae-Won Kang

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BACKGROUNDS Epidermolysis bullosa simplex (EBS) is a group of hereditary bullous disorders caused by mutations in the keratin genes KRT5 and KRT14. A significant genotype-phenotype correlation has been noted in previous studies of EBS. OBJECTIVE In order to identify additional EBS mutations and elucidate the genotype-phenotype correlations in Korean EBS(More)
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