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Severe epidermolysis bullosa simplex phenotype caused by codominant mutations p.Ile377Thr in keratin 14 and p.Gly138Glu in keratin 5.

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Title: Severe epidermolysis bullosa simplex phenotype caused by codominant mutations p.Ile377Thr in keratin 14 and p.Gly138Glu in keratin 5.
Authors: Bchetnia, Mbarka1 (AUTHOR), Allard, Jean‐Pascal2 (AUTHOR), Boucher‐Lafleur, Anne‐Marie1 (AUTHOR), Cruz Marino, Tania2 (AUTHOR), Dupéré, Audrey2 (AUTHOR), Powell, Julie3 (AUTHOR), McCuaig, Catherine3 (AUTHOR), Bernier, Marie‐Ève2 (AUTHOR), Laprise, Catherine1,2 (AUTHOR) catherine.laprise@uqac.ca
Source: Experimental Dermatology. Oct2020, Vol. 29 Issue 10, p961-969. 9p.
Database: Academic Search Ultimate
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ISSN:09066705
DOI:10.1111/exd.14189