Carregant...
PTPN11-Associated Mutations in the Heart: Has LEOPARD changed its RASpots?
In this review, we focus on elucidating the cardiac function of germline mutations in the PTPN11 gene, encoding the SH2 domain-containing protein tyrosine phosphatase SHP2. PTPN11 mutations cause LEOPARD Syndrome (LS) and Noonan Syndrome (NS), two disorders that are part of a newly classified family...
Guardat en:
| Autors principals: | , |
|---|---|
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2011
|
| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3372917/ https://ncbi.nlm.nih.gov/pubmed/22681964 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.tcm.2012.03.006 |
| Etiquetes: |
Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!
|