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Identification of Novel Causal FBN1 Mutations in Pedigrees of Marfan Syndrome
Marfan syndrome (MFS) is an autosomal dominant genetic disorder of the connective tissue, typically characteristic of cardiovascular manifestations, valve prolapse, left ventricle enlargement, and cardiac failure. Fibrillin-1 (FBN1) is the causative gene in the pathogenesis of MFS. Patients with dif...
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| Publicado no: | Int J Genomics |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Hindawi
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5932419/ https://ncbi.nlm.nih.gov/pubmed/29850472 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2018/1246516 |
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