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Systematic mutation screening of KRT5 supports the hypothesis that Galli–Galli disease is a variant of Dowling–Degos disease.
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- British Journal of Dermatology, 2010, v. 163, n. 1, p. 197, doi. 10.1111/j.1365-2133.2010.09741.x
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- Article
A novel KRT86 mutation in a Turkish family with monilethrix, and identification of maternal mosaicism.
- Published in:
- Clinical & Experimental Dermatology, 2015, v. 40, n. 7, p. 781, doi. 10.1111/ced.12631
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- Article
Identification of a U2HR gene mutation in Turkish families with Marie Unna hereditary hypotrichosis.
- Published in:
- Clinical & Experimental Dermatology, 2009, v. 34, n. 8, p. e953, doi. 10.1111/j.1365-2230.2009.03644.x
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- Article