Severe epidermolysis bullosa simplex phenotype caused by codominant mutations p.Ile377Thr in keratin 14 and p.Gly138Glu in keratin 5
Bchetnia, Mbarka, Allard, JeanâPascal, BoucherâLafleur, AnneâMarie, Cruz Marino, Tania, Dupéré, Audrey, Powell, Julie, McCuaig, Catherine, Bernier, MarieâÃve, Laprise, CatherineJournal:
Experimental Dermatology
DOI:
10.1111/exd.14189
Date:
September, 2020
File:
PDF, 16.28 MB
2020