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    Molecular Genetics of Keratinization Disorders: What's New About Ichthyosis

    January 2020 in “ Acta dermato-venereologica
    Jouni Uitto, Leila Youssefian, Amir Hossein Saeidian, Hassan Vahidnezhad
    Studysummary This overview discusses advancements in the understanding of molecular genetics in heritable keratinization disorders, focusing on recent cases of inherited ichthyosis, and reports no new clinical results.
    Automatically generated from the study's abstract, not written by a person, and not a review of the full paper. Not medical advice or a treatment recommendation. Read the original study, and consult a qualified healthcare professional before changing treatment. Full disclaimer
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    Research cited in this study 2

    1. A Novel Mutation in ST14 at a Functionally Significant Amino Acid Residue Expands the Spectrum of Ichthyosis-Hypotrichosis Syndrome Orphanet Journal of Rare Diseases · 2017
    2. Inherited Ichthyoses: Generalized Mendelian Disorders of Cornification European journal of human genetics · 2012