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Polussa J, Schneider A, Hagerman R. Molecular Advances Leading to Treatment Implications for Fragile X Premutation Carriers. Brain Disord Ther. 2014;3doi: 10.4172/2168-975X.1000119.
Polussa, J., Schneider, A., & Hagerman, R. (2014). Molecular Advances Leading to Treatment Implications for Fragile X Premutation Carriers. Brain disorders & therapy, 3. https://doi.org/10.4172/2168-975X.1000119
Polussa, Jonathan, et al. "Molecular Advances Leading to Treatment Implications for Fragile X Premutation Carriers." Brain disorders & therapy vol. 3 (2014). doi: https://doi.org/10.4172/2168-975X.1000119
Polussa J, Schneider A, Hagerman R. Molecular Advances Leading to Treatment Implications for Fragile X Premutation Carriers. Brain Disord Ther. 2014;3. doi: 10.4172/2168-975X.1000119. PMID: 25436181; PMCID: PMC4245015.
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Brain Disord Ther. 2014;3. doi: 10.4172/2168-975X.1000119.

Molecular Advances Leading to Treatment Implications for Fragile X Premutation Carriers.

Brain disorders & therapy

Jonathan Polussa, Andrea Schneider, Randi Hagerman

Affiliations

  1. Medical Investigation of Neurodevelopmental Disorders (MIND) Institute, University of California Davis Health System, Sacramento, California, USA ; Department of Pediatrics, University of California Davis Health System, Sacramento, California, USA.

PMID: 25436181 PMCID: PMC4245015 DOI: 10.4172/2168-975X.1000119

Abstract

Fragile X syndrome (FXS) is the most common single gene cause of intellectual disability and it is characterized by a CGG expansion of more than 200 repeats in the

Keywords: Aging; Antioxidants; FMR1; FMRP; FXTAS; Fragile X premutation; Oxidative stress; Treatment

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