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Mutations in PTPN11, encoding the protein tyrosine phosph... | ResearchHub
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Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome
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Authors
Marco Tartaglia
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Marco Tartaglia
•
Hannie Kremer
15 more
•
Bruce Gelb
Published
November 12, 2001
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Journal
Nature Genetics
Topics
Biology
Immunology
Molecular Biology
Mutation
Noonan Syndrome
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DOI
10.1038/ng772
