The recurrent PPP1CB mutation p.Pro49Arg in an additional Noonan‐like syndrome individual: Broadening the clinical phenotype

Overview of attention for article published in American Journal of Medical Genetics. Part A, February 2017

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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

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