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• Provides a comprehensive overview of the molecular genetics, clinical trials, and treatment of Fragile X Syndrome
• Written for academic researchers, pharmaceutical investigators, and clinicians in the field
• Edited by international leaders in the field who have contributed greatly to the study of Fragile X Syndrome
• Directs the reader through complex issues surrounding FXS and draws the literature together for researchers and clinicians
Authors
• Rob Willemsen, Department of Clinical Neurogenetics, Erasmus University Medical Center, Rotterdam, The
• Netherlands Frank Kooy, Department of Medical Genetics, University of Antwerp, Antwerp, Belgium