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1. Confirmation of the role of a KRT5 mutation and successful management of skin lesions in a patient with Galli-Galli disease.

Author

Lőrincz K, Medvecz M, Kiss N, Glász-Bóna A, Hársing J, Lepesi-Benkő R, Hatvani Z, Mazán M, Kárpáti S, and Wikonkál N

Subjects
Acantholysis drug therapy, Acitretin therapeutic use, Aged, Humans, Keratolytic Agents therapeutic use, Male, Recurrence, Acantholysis genetics, Frameshift Mutation genetics, Keratin-5 genetics
Published
2018
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