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  3. Mutation in exon 1a of PLEC, leading to disruption of plectin isoform 1a, causes autosomal-recessive skin-only epidermolysis bullosa simplex
 

Mutation in exon 1a of PLEC, leading to disruption of plectin isoform 1a, causes autosomal-recessive skin-only epidermolysis bullosa simplex

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BORIS DOI
10.7892/boris.115731
Date of Publication
2015
Publication Type
Article
Division/Institute

Universitätsklinik fü...

Contributor
Gostyńska, Katarzyna B.
Nijenhuis, Miranda
Lemmink, Henny
Pas, Hendri H.
Pasmooij, Anna M.G.
Kernland Lang, Kristin Helene
Universitätsklinik für Dermatologie
Castañón, Maria J.
Wiche, Gerhard
Jonkman, Marcel F.
Subject(s)

600 - Technology::610...

Series
Human molecular genetics
ISSN or ISBN (if monograph)
0964-6906
Publisher
Oxford University Press
Language
English
Publisher DOI
10.1093/hmg/ddv066
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/161405
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