Associated Papers
First Case of KRT2 Epidermolytic Nevus and Novel Clinical and Genetic Findings in 26 Italian Patients with Keratinopathic Ichthyoses.
Diociaiuti A et al.
International Journal of Molecular Sciences, 2020
Recurrent KRT10 Variant in Ichthyosis with Confetti.
Takeichi T et al.
Acta Dermato-venereologica, 2020
Chromosomal inversions as a hidden disease-modifying factor for somatic recombination phenotypes.
Nomura T et al.
Jci Insight, 2018
Predictive phenotyping of inherited ichthyosis by next-generation DNA sequencing.
Saito R et al.
The British Journal of Dermatology, 2017
Expanding the Clinical and Genetic Spectrum of KRT1, KRT2 and KRT10 Mutations in Keratinopathic Ichthyosis.
Hotz A et al.
Acta Dermato-venereologica, 2016
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