SHP nonreceptor protein tyrosine 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
- NSML, SHP
- Genetics
- https://doi.org/10.1038/ng772