Src homology 2 domain-containing phosphatase(English)
- missense mutations in PTPN11 (MIM 176876) of this gene, which contains two Src homology 2 (SH2) domains, cause Noonan syndrome and account for more than 50% of the cases. Also as SHP-2
- IFN-γ, NSML, PTPN1, SHP, YAP
- Genetics, Cardiology
- https://doi.org/10.1038/ng772
- https://doi.org…093/cvr/cvag177