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Marfan syndrome: An eyesight of syndrome()
Marfan syndrome (MFS), a relatively common autosomal dominant hereditary disorder of connective tissue with prominent manifestations in the skeletal, ocular, and cardiovascular systems, is caused by mutations in the glycoprotein gene fibrillin-1 (FBN1). Aortic root dilation and mitral valve prolapse...
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| Gepubliceerd in: | Meta Gene |
|---|---|
| Hoofdauteurs: | , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Elsevier
2014
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4287801/ https://ncbi.nlm.nih.gov/pubmed/25606393 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.mgene.2013.10.008 |
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