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SMAD4 rare variants in individuals and families with thoracic aortic aneurysms and dissections
SMAD4 pathogenic variants cause juvenile polyposis (JPS) and hereditary hemorrhagic telangiectasia (HHT), and 40% of affected individuals also have thoracic aortic disease. At the same time, SMAD4 pathogenic variants have not been reported in thoracic aortic disease families without JPS-HHT. A SMAD4...
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| Publicado no: | Eur J Hum Genet |
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| Main Authors: | , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer International Publishing
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6777456/ https://ncbi.nlm.nih.gov/pubmed/30809044 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41431-019-0357-x |
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