Determination of the molecular basis of Marfan syndrome: a growth industry
Although it has been known for more than a decade that Marfan syndrome — a dominantly inherited connective tissue disorder characterized by tall stature, arachnodactyly, lens subluxation, and a high risk of aortic aneurysm and dissection — results from mutations in the FBN1 gene, which encodes fibri...
Guardat en:
| Publicat a: | J Clin Invest |
|---|---|
| Autor principal: | |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
American Society for Clinical Investigation
2004
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC449756/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/15254580/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI22399 |
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