Associated Papers
The many faces of plectin and plectinopathies: pathology and mechanisms.
Winter L et al.
Acta Neuropathologica, 2013
Plectin expression patterns determine two distinct subtypes of epidermolysis bullosa simplex.
Natsuga K et al.
Human Mutation, 2010
Epidermolysis bullosa simplex associated with pyloric atresia is a novel clinical subtype caused by mutations in the plectin gene (PLEC1).
Nakamura H et al.
The Journal of Molecular Diagnostics : Jmd, 2005
Select a paper to view details