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Updated: Aug 1, 2025

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Mutagenesis and Analysis of Genetic Mutations in the GC-rich KISS1 Receptor Sequence Identified in Humans with Reproductive Disorders
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Congenital ichthyosiform erythroderma with epidermolysis due to a novel frameshift mutation in KRT10
Bernadett Kurz1, Kevin-Thomas Koschitzki1, Ute Hehr2
1Department of Dermatology, University Hospital Regensburg, Regensburg, Germany.
JAAD Case Reports
|April 27, 2023
Abstract
No abstract available in PubMed .
Keywords:
congenital ichthyosiform erythrodermafilaggrin (FLG) genekeratin 10 (KRT10) genekeratinopathic ichthyosesMore Related Videos
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