A restricted spectrum of NRAS mutations causes Noonan syndrome
Ion Cristian Cirstea(Düsseldorf University Hospital), Martin Zenker(Friedrich-Alexander-Universität Erlangen-Nürnberg), Claudio Carta(Istituto Superiore di Sanità), Torsten Merbitz-Zahradnik(Düsseldorf University Hospital), Bruno Dallapiccola(Bambino Gesù Children's Hospital), Stefan Mundlos(Max Planck Institute for Molecular Genetics), Maria Lisa Dentici(Casa Sollievo della Sofferenza), L Pennacchio(Lawrence Berkeley National Laboratory), Giuseppe Zampino(Università Cattolica del Sacro Cuore), Radovan Dvorský(Düsseldorf University Hospital), Marco Tartaglia(Bambino Gesù Children's Hospital), Denise Horn(Charité - Universitätsmedizin Berlin), Alfred Wittinghofer(Max Planck Society), Amy E. Roberts(Boston Children's Hospital), Lothar Gremer(Düsseldorf University Hospital), Liborio Stuppia(University of Chieti-Pescara), Raju Kucherlapati(Harvard University), Cesare Rossi(Policlinico S.Orsola-Malpighi), Laura Mazzanti(University of Bologna), Victoria A. Joshi(Harvard University), Kerstin Kutsche(Universität Hamburg), Cristina Digilio(Bambino Gesù Children's Hospital), Christian P. Kratz(University of Freiburg), Rainer König(Jena University Hospital), Margherita Silengo(University of Turin), Bruce D. Gelb(Icahn School of Medicine at Mount Sinai), Francesca Romana Lepri(Casa Sollievo della Sofferenza), E Seemanová(Charles University), Mohammad Reza Ahmadian(Heinrich Heine University Düsseldorf), Michael A. Patton(St George's Hospital), Francesca Pantaleoni(Istituto Superiore di Sanità)
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