Missense mutations in Desmocollin-2 N-terminus, associated with arrhythmogenic right ventricular cardiomyopathy, affect intracellular localization of desmocollin-2 in vitro

BACKGROUND: Mutations in genes encoding desmosomal proteins have been reported to cause arrhythmogenic right ventricular cardiomyopathy (ARVC), an autosomal dominant disease characterised by progressive myocardial atrophy with fibro-fatty replacement. We screened 54 ARVC probands for mutations in de...

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Detalles Bibliográficos
Autores principales: Beffagna, Giorgia, De Bortoli, Marzia, Nava, Andrea, Salamon, Michela, Lorenzon, Alessandra, Zaccolo, Manuela, Mancuso, Luisa, Sigalotti, Luca, Bauce, Barbara, Occhi, Gianluca, Basso, Cristina, Lanfranchi, Gerolamo, Towbin, Jeffrey A, Thiene, Gaetano, Danieli, Gian Antonio, Rampazzo, Alessandra
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2190757/
https://www.ncbi.nlm.nih.gov/pubmed/17963498
http://dx.doi.org/10.1186/1471-2350-8-65

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2190757/
https://www.ncbi.nlm.nih.gov/pubmed/17963498
http://dx.doi.org/10.1186/1471-2350-8-65

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