The molecular mechanism underlying Roberts syndrome involves loss of ESCO2 acetyltransferase activity

Miriam Gordillo, Hugo Vega, Alison H. Trainer, Fajian Hou, Norio Sakai, Ricardo Luque, Hülya Kayserili, Seher Basaran, Flemming Skovby, Raoul C M Hennekam, Maria L Giovannucci Uzielli, Rhonda E. Schnur, Sylvie Manouvrier, Susan Chang, Edward Blair, Jane A. Hurst, Francesca Forzano, Moritz Meins, Kalle O J Simola, Annick Raas-rothschildRoger A. Schultz, Lisa D. Mcdaniel, Keiichi Ozono, Koji Inui, Hui Zou, Ethylin Wang Jabs

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