Protein synthesis levels are increased in a subset of individuals with fragile X syndrome

Author:

Jacquemont Sébastien12,Pacini Laura3,Jønch Aia E45,Cencelli Giulia3,Rozenberg Izabela6,He Yunsheng7,D’Andrea Laura3,Pedini Giorgia3,Eldeeb Marwa8,Willemsen Rob9,Gasparini Fabrizio10,Tassone Flora11,Hagerman Randi12,Gomez-Mancilla Baltazar613,Bagni Claudia314ORCID

Affiliation:

1. Sainte-Justine University Hospital Research Centre, Montreal, QC, Canada

2. University of Montreal, Montreal, QC, Canada

3. Department of Biomedicine and Prevention, University of Rome Tor Vergata, Rome, Italy

4. Department of Clinical Genetics, Odense University Hospital, Odense, Denmark

5. Human Genetics, Department of Clinical Research, University of Southern Denmark, Odense, Denmark

6. Neuroscience Translational Medicine, Novartis Institutes for Biomedical Research, Novartis Pharma AG, Basel, Switzerland

7. Biomarker Development, Novartis Institutes for Biomedical Research, Cambridge, MA, USA

8. Medical Investigation of Neurodevelopmental Disorders (MIND) Institute, University of California, Davis Medical Center, Sacramento, CA, USA

9. Department of Clinical Genetics, Erasmus Medical Center, 1738, Rotterdam, The Netherlands

10. Neuroscience Discovery, Novartis Institutes for BioMedical Research, Basel, Switzerland

11. Department of Biochemistry and Molecular Medicine and Medical Investigation of Neurodevelopmental Disorders (MIND) Institute, Sacramento, CA, USA

12. Department of Pediatric and Medical Investigation of Neurodevelopmental Disorders (MIND) Institute, University of California Davis, School of Medicine, Sacramento, CA, USA

13. Department of Neurology and Neurosurgery, McGill University, Montreal, QC, Canada

14. Department of Fundamental Neuroscience, University of Lausanne, Lausanne, Switzerland

Funder

Jerome Lejeune Foundation

National Institute of Child Health and Human Development

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

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