Distribution of ichthyin mutations in patients with ARCI with EM type III | Download Table
Autosomal Recessive Congenital Ichthyosis | Actas Dermo-Sifiliográficas
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Molecular epidemiology of non‐syndromic autosomal recessive congenital ichthyosis in a Middle‐Eastern population - Mohamad - 2021 - Experimental Dermatology - Wiley Online Library
Ichthyosis molecular fingerprinting shows profound TH17 skewing and a unique barrier genomic signature. - Abstract - Europe PMC
A multicenter study on quality of life of the “greater patient” in congenital ichthyoses | Orphanet Journal of Rare Diseases | Full Text
Lamellar Ichthyosis (autosomal recessive congenital ichthyosis, ARCI) - Neurology Advisor
Distinct skin microbiome community structures in congenital ichthyosis - Tham - 2022 - British Journal of Dermatology - Wiley Online Library
Mutations in transglutaminase 1 gene in autosomal recessive congenital ichthyosis in Egyptian families
Pleomorphic Ichthyosis: Proposed Name for a Heterogeneous Group of Congenital Ichthyoses with Phenotypic Shifting and Mild Residual Scaling | HTML | Acta Dermato-Venereologica
The Major Orphan Forms of Ichthyosis Are Characterized by Systemic T-Cell Activation and Th-17/Tc-17/Th-22/Tc-22 Polarization in Blood - ScienceDirect
Novel CYP4F22 mutations associated with autosomal recessive congenital ichthyosis (ARCI). Study of the CYP4F22 c.1303C>T founder mutation | PLOS ONE
Novel CYP4F22 mutations associated with autosomal recessive congenital ichthyosis (ARCI). Study of the CYP4F22 c.1303C>T founder mutation | PLOS ONE
Autosomal recessive congenital ichthyosis - Altmeyers Encyclopedia - Department Dermatology
Neha Singh Vandana Bansal* Tejaswini Patil Kaizad Damania ABSTRACT KEYWORDS INTERNATIONAL JOURNAL OF SCIENTIFIC RESEARCH
Characteristics of the five ARCI patients with TGM1 mutations included... | Download Table
Pleomorphic Ichthyosis: Proposed Name for a Heterogeneous Group of Congenital Ichthyoses with Phenotypic Shifting and Mild Residual Scaling | HTML | Acta Dermato-Venereologica
Autosomal Recessive Congenital Ichthyosis in American Bulldogs Is Associated With NIPAL4 (ICHTHYIN) Deficiency - E. A. Mauldin, P. Wang, E. Evans, C. A. Cantner, J. D. Ferracone, K. M. Credille, M. L. Casal, 2015
A Japanese Case of Ichthyosiform Erythroderma with a Novel Mutation in NIPAL4/Ichthyin | HTML | Acta Dermato-Venereologica
Inherited clinical disorders of lipid metabolism. | Semantic Scholar
A, Venn diagram showing DEGs comparing ichthyosis subtypes: NS, LI,... | Download Scientific Diagram
Novel CYP4F22 mutations associated with autosomal recessive congenital ichthyosis (ARCI). Study of the CYP4F22 c.1303C>T founder mutation | PLOS ONE
