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A novel FBN1 mutation causes autosomal dominant Marfan syndrome
Marfan syndrome (MFS) is an inherited and systemic disorder. It has been reported that mutations in the fibrillin-1 gene (FBN1) account for ~90% of autosomal dominant cases of MFS. This study was conducted to screen mutations of FBN1 in a Chinese family with autosomal dominant MFS; four individuals...
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| Publicado no: | Mol Med Rep |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
D.A. Spandidos
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5865861/ https://ncbi.nlm.nih.gov/pubmed/28944857 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/mmr.2017.7544 |
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