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 Nature Genet. 29, 465–468 (2001).
The locus for Noonan syndrome was incorrectly referred to as N-SH2, in the introductory paragraph. The third sentence of the paragraph should read: “It has been mapped to a 5-cM region (NS1) on chromosome 12q24.1, and genetic heterogeneity has also been documented3–6.”
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The online version of the original article can be found at 10.1038/ng772
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Erratum: Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome. Nat Genet 30, 123 (2002). https://doi.org/10.1038/ng0102-123d
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DOI: https://doi.org/10.1038/ng0102-123d
