Protein synthesis levels are increased in a subset of individuals with fragile X syndrome.
Resource Type
Academic Journal
Authors
Jacquemont S; Sainte-Justine University Hospital Research Centre, Montreal, QC H3T 1C5.; University of Montreal, Montreal, QC H3T 1J4, Canada.; Pacini L; Department of Biomedicine and Prevention, University of Rome Tor Vergata, Rome, Italy.; Jønch AE; Department of Clinical Genetics, Odense University Hospital.; Human Genetics, Department of Clinical Research, University of Southern Denmark, 5000 Odense, Denmark.; Cencelli G; Department of Biomedicine and Prevention, University of Rome Tor Vergata, Rome, Italy.; Rozenberg I; Neuroscience Translational Medicine, Novartis Institutes for Biomedical Research, Novartis Pharma AG, Basel, Switzerland.; He Y; Biomarker Development, Novartis Institutes for Biomedical Research, Cambridge, MA, USA.; D'Andrea L; Department of Biomedicine and Prevention, University of Rome Tor Vergata, Rome, Italy.; Pedini G; Department of Biomedicine and Prevention, University of Rome Tor Vergata, Rome, Italy.; Eldeeb M; Medical Investigation of Neurodevelopmental Disorders (MIND) Institute, University of California, Davis Medical Center, Sacramento, CA, USA.; Willemsen R; Department of Clinical Genetics, Erasmus Medical Center, DRRotterdam, Netherlands.; Gasparini F; Neuroscience Discovery, Novartis Institutes for BioMedical Research, Basel, Switzerland.; Tassone F; Department of Biochemistry and Molecular Medicine and Medical Investigation of Neurodevelopmental Disorders (MIND) Institute.; Hagerman R; Department of Pediatric and Medical Investigation of Neurodevelopmental Disorders (MIND) Institute, University of California Davis, School of Medicine, Sacramento, CA, USA.; Gomez-Mancilla B; Neuroscience Translational Medicine, Novartis Institutes for Biomedical Research, Novartis Pharma AG, Basel, Switzerland.; Department of Neurology and Neurosurgery, McGill University, Montreal, Canada.; Bagni C; Department of Biomedicine and Prevention, University of Rome Tor Vergata, Rome, Italy.; Department of Fundamental Neuroscience, University of Lausanne, Lausanne, Switzerland.
Source
Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: PubMed not MEDLINE