Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome
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Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome
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(P356) |
10.1038/NG772
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(P698) |
11704759
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(P3181) |
2152387
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(P5875) |
11649659
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(P6179) |
1020342806
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