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Genetic analysis of the contribution of LTBP-3 to thoracic aneurysm in Marfan syndrome
Marfan syndrome (MFS) is an autosomal dominant disorder of connective tissue, caused by mutations of the microfibrillar protein fibrillin-1, that predisposes affected individuals to aortic aneurysm and rupture and is associated with increased TGFβ signaling. TGFβ is secreted from cells as a latent c...
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| Publicado no: | Proc Natl Acad Sci U S A |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
National Academy of Sciences
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4653215/ https://ncbi.nlm.nih.gov/pubmed/26494287 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1507652112 |
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