Clinical and Genetic Investigation of Ichthyosis in Familial and Sporadic Cases in Southern Tunisia: Genotype–Phenotype Correlation

    January 2022 in “ BMC Medical Genomics
    Mariem Ennouri, Andreas Zimmer, E. Bahloul, R. Chaabouni, Slaheddine Marrakchi, H. Turki, Faiza Fakhfakh, Noura Bougacha‐Elleuch, Judith Fischer
    Studysummary This study identified eight mutations in five genes associated with different aspects of ichthyosis among Tunisian patients, enhancing understanding of its genetic and clinical diversity.
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