403 followers
The recurrent PPP1CB mutation p.Pro49Arg in an additional Noonan-like syndrome individual https://t.co/d2PslMvFEO
The recurrent PPP1CB mutation p.Pro49Arg in an additional Noonan-like syndrome individual https://t.co/d2PslMvFEO
PPP1CB P49R mutation in Noonan-like syndrome with craniosynostosis. Expanding the spectrum of rasopathies. https://t.co/L5AMODQiCg