Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome

Marco Tartaglia(Istituto Superiore di Sanità), Ernest L. Mehler(Icahn School of Medicine at Mount Sinai), Rosalie Goldberg(Albert Einstein College of Medicine), Giuseppe Zampino(Università Cattolica del Sacro Cuore), Han G. Brunner(Radboud University Nijmegen), Hannie Kremer(Radboud University Medical Center), Ineke van der Burgt(Radboud University Medical Center), Andrew H. Crosby(St George's Hospital), Andra Ion(St George's Hospital), Steve Jeffery(St George's Hospital), Kamini Kalidas(St George's Hospital), Michael A. Patton(St George's Hospital), Raju Kucherlapati(Albert Einstein College of Medicine), Bruce D. Gelb(Icahn School of Medicine at Mount Sinai)
Nature Genetics
November 12, 2001
Cited by 1,735

Abstract


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