Associated Papers
Phenotypic variability in gap junction syndromic skin disorders: experience from KID and Clouston syndromes' clinical diagnostics.
Kutkowska-Kaźmierczak A et al.
Journal of Applied Genetics, 2015
Buschke-Ollendorff syndrome associated with hypertrophic scar formation: a possible role for LEMD3 mutation.
Korekawa A et al.
The British Journal of Dermatology, 2012
Possible modifier effects of keratin 17 gene mutation on keratitis-ichthyosis-deafness syndrome.
Natsuga K et al.
The British Journal of Dermatology, 2012
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