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Congenital ichthyosiform erythroderma with epidermolysis due to a novel frameshift mutation in KRT10

Congenital ichthyosiform erythroderma with epidermolysis due to a novel frameshift mutation in KRT10

Bibliographic Details
Main Authors: Bernadett Kurz, MD, Kevin-Thomas Koschitzki, MD, Ute Hehr, MD, Ute Germer, MD, Julia Schreml, MD, Florian Langhammer, MD, Stephan Schreml, MD
Format: Article
Language:English
Published: Elsevier 2023-05-01
Series:JAAD Case Reports
Subjects:
congenital ichthyosiform erythroderma
filaggrin (FLG) gene
keratin 10 (KRT10) gene
keratinopathic ichthyoses
Online Access:http://www.sciencedirect.com/science/article/pii/S2352512623000929
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http://www.sciencedirect.com/science/article/pii/S2352512623000929

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