Severe epidermolysis bullosa simplex phenotype caused by codominant mutations p.Ile377Thr in keratin 14 and p.Gly138Glu in keratin 5. - Bchetnia, Mbarka; Allard, Jean‐Pascal; Boucher‐Lafleur, Anne‐Marie; Cruz Marino, Tania; Dupéré, Audrey; Powell, Julie; McCuaig, Catherine; Bernier, Marie‐Ève; Laprise, Catherine (Experimental Dermatology, 2020)