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Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome.
M Tartaglia, E L Mehler, R Goldberg, G Zampino, H G Brunner, H Kremer, I van der Burgt, A H Crosby, A Ion, S Jeffery, K Kalidas, M A Patton, R S Kucherlapati, B D Gelb
Nat Genet 2001; 29(4):465-468
ICID: 841251
IC™ Value: 40.91
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