A carregar...
Emerging roles of BMP9 and BMP10 in hereditary hemorrhagic telangiectasia
Rendu–Osler–Weber syndrome, also known as hereditary hemorrhagic telangiectasia (HHT), is an autosomal dominant vascular disorder. Three genes are causally related to HHT: the ENG gene encoding endoglin, a co-receptor of the TGFβ family (HHT1), the ACVRL1 gene encoding ALK1 (activin receptor-like ki...
Na minha lista:
| Publicado no: | Front Genet |
|---|---|
| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Frontiers Media S.A.
2015
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4288046/ https://ncbi.nlm.nih.gov/pubmed/25620979 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2014.00456 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|