Title : Epidermolysis bullosa simplex in Japanese and Korean patients: genetic studies in 19 cases.

Pub. Date : 2006 Aug

PMID : 16882168






1 Functional Relationships(s)
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1 BACKGROUND: Epidermolysis bullosa simplex (EBS) comprises a group of hereditary bullous diseases characterized by intraepidermal blistering caused by mutations in either keratin gene, KRT5 or KRT14. simplex keratin 5 Homo sapiens