Modeling (not so) rare developmental disorders associated with mutations in the protein-tyrosine phosphatase SHP2
Maja Šolman(University Medical Center Utrecht), Jeroen den Hertog(Leiden University)
Cited by 11
Related Papers
Dimerization of Receptor Protein-Tyrosine Phosphatase alpha in living cells
|BMC Cell Biology|2001|92
Heterozygous germline mutations in A2ML1 are associated with a disorder clinically related to Noonan syndrome
|European Journal of Human Genetics|2014|75