A carregar...
Co-expression of FBN1 with mesenchyme-specific genes in mouse cell lines: implications for phenotypic variability in Marfan syndrome
Mutations in the human FBN1 gene cause Marfan syndrome, a complex disease affecting connective tissues but with a highly variable phenotype. To identify genes that might participate in epistatic interactions with FBN1, and could therefore explain the observed phenotypic variability, we have looked f...
Na minha lista:
| Main Authors: | , , , , |
|---|---|
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group
2010
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2987476/ https://ncbi.nlm.nih.gov/pubmed/20551991 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2010.91 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|