The fragile X syndrome: exploring its molecular basis and seeking a treatment
The fragile X syndrome: exploring its molecular basis and seeking a treatment
About this item
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Publisher
Cambridge, UK: Cambridge University Press
Journal title
Language
English
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Publisher
Cambridge, UK: Cambridge University Press
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Scope and Contents
Contents
Fragile X syndrome (FXS) – the leading cause of inherited mental retardation – is an X-linked disease caused by loss of expression of the FMR1 (fragile X mental retardation 1) gene. In addition to impairment of higher-cognitive functions, FXS patients show a variety of physical and other mental abnormalities. FMRP, the protein encoded by the FMR1 g...
Alternative Titles
Full title
The fragile X syndrome: exploring its molecular basis and seeking a treatment
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TN_cdi_proquest_miscellaneous_67887899
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_67887899
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ISSN
1462-3994
E-ISSN
1462-3994
DOI
10.1017/S1462399406010751
