Marfan syndrome: current perspectives

Marfan syndrome (MFS) is a pleiotropic connective tissue disease inherited as an autosomal dominant trait, due to mutations in the FBN1 gene encoding fibrillin 1. It is an important protein of the extracellular matrix that contributes to the final structure of a microfibril. Few cases displaying an...

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Detalles Bibliográficos
Autores principales: Pepe, Guglielmina, Giusti, Betti, Sticchi, Elena, Abbate, Rosanna, Gensini, Gian Franco, Nistri, Stefano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2016
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4869846/
https://www.ncbi.nlm.nih.gov/pubmed/27274304
http://dx.doi.org/10.2147/TACG.S96233

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4869846/
https://www.ncbi.nlm.nih.gov/pubmed/27274304
http://dx.doi.org/10.2147/TACG.S96233

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