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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-rothschild
*Corresponding author for this work
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- Oxford University Hospitals NHS Foundation Trust
- E.O. Ospedali Galliera
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- University of Texas Southwestern Medical Center
Research output: Contribution to journal › Article › peer-review
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