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Browsing Internal Medicine by Subject "Epidermolysis bullosa simplex"

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A novel keratin 5 mutation in an African family with epidermolysis bullosa simplex Iidicates the Importance of the amino acid located at the boundary site between the H1 and coil 1A domains

Shinkuma, Satoru; Nishie, Wataru; Jacyk, Witold Kamil; Natsuga, Ken; Ujiie, Hideyuki; Nakamura, Hideki; Akiyama, Masashi; Shimizu, Hiroshi (Medical Journals, 2013-09)

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