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Loss-of-function mutations in TGFB2 cause a syndromic presentation of thoracic aortic aneurysm
Loeys-Dietz syndrome (LDS) associates with a tissue signature for high transforming growth factor (TGF)-β signaling but is often caused by heterozygous mutations in genes encoding positive effectors of TGF-β signaling, including either subunit of the TGF-β receptor or SMAD3, thereby engendering cont...
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| Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3616632/ https://ncbi.nlm.nih.gov/pubmed/22772368 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ng.2349 |
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