Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives

    Mbarka Bchetnia, Julie Powell, Catherine McCuaïg, Anne‐Marie Boucher‐Lafleur, Charles Morin, Audrey Dupéré, Catherine Laprise
    Studysummary This review explores epidermolysis bullosa simplex subtypes caused by mutations in <i>KRT5</i> or <i>KRT14</i> and summarizes gene expression patterns and molecular mechanisms, without presenting new experimental results.
    Our plain-language summary. Not medical advice or a treatment recommendation. Consult a qualified healthcare professional before changing treatment. Full disclaimer
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