Mutation of SHOC2 promotes aberrant protein N-myristoylation and causes Noonan-like syndrome with loose anagen hair
Viviana Cordeddu(Istituto Superiore di Sanità), Marco Tartaglia(Bambino Gesù Children's Hospital), M. Cristina Digilio(Bambino Gesù Children's Hospital), Serena Cecchetti(Istituto Superiore di Sanità), Martin Zenker(Otto-von-Guericke-Universität Magdeburg), Simone Martinelli(Istituto Superiore di Sanità), Cecilia Anichini(University of Siena), Deborah Bartholdi(University of Zurich), L Pennacchio(Lawrence Berkeley National Laboratory), Avi Ma’ayan(Icahn School of Medicine at Mount Sinai), Anna Lipzen(Lawrence Berkeley National Laboratory), Elia Di Schiavi(National Research Council), Giuseppe Zampino(Università Cattolica del Sacro Cuore), Angelo Selicorni(Fondazione Roma), Anna Sárközy(Great Ormond Street Hospital), Wendy Schackwitz(Joint Genome Institute), Daniela Merlo(Istituto Superiore di Sanità), Ravi Iyengar(Institute for Biomedicine), Cesare Rossi(Policlinico S.Orsola-Malpighi), Laura Mazzanti(University of Bologna), Romano Tenconi(University of Padua), Joel Martin(Joint Genome Institute), Alessio Cardinale(IRCCS Ospedale San Raffaele), Kerstin Kutsche(Universität Hamburg), Paolo Bazzicalupo(Institute of Genetics and Biophysics), Valentina Fodale(IRBM Science Park), Bruce D. Gelb(Child Health and Development Institute), Elisabetta Flex(Istituto Superiore di Sanità), Giovanni Battista Ferrero(5T Torino (Italy)), Francesca Romana Lepri(Casa Sollievo della Sofferenza), Bruno Dallapiccola(Bambino Gesù Children's Hospital)
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