The rod domain is not essential for the function of plectin in maintaining tissue integrity

Epidermolysis bullosa simplex associated with late-onset muscular dystrophy (EBS-MD) is an autosomal recessive disorder resulting from mutations in the plectin gene. The majority of these mutations occur within the large exon 31 encoding the central rod domain and leave the production of a low-level...

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Detalles Bibliográficos
Autores principales: Ketema, Mirjam, Secades, Pablo, Kreft, Maaike, Nahidiazar, Leila, Janssen, Hans, Jalink, Kees, de Pereda, Jose M., Sonnenberg, Arnoud
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2015
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4571296/
https://www.ncbi.nlm.nih.gov/pubmed/25971800
http://dx.doi.org/10.1091/mbc.E15-01-0043

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4571296/
https://www.ncbi.nlm.nih.gov/pubmed/25971800
http://dx.doi.org/10.1091/mbc.E15-01-0043

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