Molecular medicine of fragile X syndrome: based on known molecular mechanisms
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology and Child Health
Link
http://link.springer.com/content/pdf/10.1007/s12519-015-0052-0.pdf
Reference94 articles.
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2. Hunter J, Rivero-Arias O, Angelov A, Kim E, Fotheringham I, Leal J. Epidemiology of fragile X syndrome: a systematic review and meta-analysis. Am J Med Genet A 2014;164A:1648–1658.
3. Wang T, Bray SM, Warren ST. New perspectives on the biology of fragile X syndrome. Curr Opin Genet Dev 2012;22:256–263.
4. Reiss AL, Hall SS. Fragile X syndrome: assessment and treatment implications. Child Adolesc Psychiatr Clin N Am 2007;16:663–675.
5. Hatton DD, Hooper SR, Bailey DB, Skinner ML, Sullivan KM, Wheeler A. Problem behavior in boys with fragile X syndrome. Am J Med Genet 2002;108:105–116.
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1. Reactivation of FMR1 gene expression is a promising strategy for fragile X syndrome therapy;Gene Therapy;2020-03-12
2. Non-coding RNA in Fragile X Syndrome and Converging Mechanisms Shared by Related Disorders;Frontiers in Genetics;2019-03-01
3. Multifarious Functions of the Fragile X Mental Retardation Protein;Trends in Genetics;2017-10
4. The mechanism of action of FXR1P-related miR-19b-3p in SH-SY5Y;Gene;2016-08
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