First Case of <i>KRT2</i> Epidermolytic Nevus and Novel Clinical and Genetic Findings in 26 Italian Patients with Keratinopathic Ichthyoses
Keratinopathic ichthyoses (KI) are a clinically heterogeneous group of keratinization disorders due to mutations in <i>KRT1</i>, <i>KTR10</i>, or <i>KRT2</i> genes encoding keratins of suprabasal epidermis. Characteristic clinical features include superficial blis...
Main Authors: | , , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
MDPI AG
2020-10-01
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Series: | International Journal of Molecular Sciences |
Subjects: | |
Online Access: | https://www.mdpi.com/1422-0067/21/20/7707 |