Transgenic Mice Expressing a Mutant Form of Loricrin Reveal the Molecular Basis of the Skin Diseases, Vohwinkel Syndrome and Progressive Symmetric Erythrokeratoderma

Mutations in the cornified cell envelope protein loricrin have been reported recently in some patients with Vohwinkel syndrome (VS) and progressive symmetric erythrokeratoderma (PSEK). To establish a causative relationship between loricrin mutations and these diseases, we have generated transgenic m...

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Detalles Bibliográficos
Autores principales: Suga, Yasushi, Jarnik, Michal, Attar, Paul S., Longley, Mary A., Bundman, Donnie, Steven, Alasdair C., Koch, Peter J., Roop, Dennis R.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2000
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2192631/
https://www.ncbi.nlm.nih.gov/pubmed/11038186

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2192631/
https://www.ncbi.nlm.nih.gov/pubmed/11038186

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