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erythrokeratodermas
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Skin biopsies from patients with ichthyosis subtypes
OMIM - Cole disease
OMIM - Huriez syndrome
OMIM - MEDNIK syndrome
OMIM - Vohwinkel syndrome
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Erythrokeratoderma variabilis (EKV) - First Nepalese case documenting GJB3 mutation.
Analysis of TYR Gene Pathogenic Variants in a Chinese Mongolian Family with Progressive Symmetric Er…
Confirming the recessive inheritance of PERP-related erythrokeratoderma.
Integration of Phenotype Term Prioritization and Gene Expression Analysis Reveals a Novel Variant in…
Fulminant myocarditis following recurrent generalized erythrokeratoderma in a child with a heterozyg…
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National Registry for Ichthyosis and Related Disorders
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