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An enormous Italian pedigree of Marfan syndrome with a novel mutation in the FBN1 gene
We characterize a large Italian family presenting with Marfan syndrome (MFS), where the same NM_000138.4:c.6872‐1G > T splice site mutation in the FBN1 gene was detected in 37 affected individuals with different pathological phenotypes. Further studies on such a large pedigree could identify othe...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7455403/ https://www.ncbi.nlm.nih.gov/pubmed/32884772 http://dx.doi.org/10.1002/ccr3.2881 |