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Characterization and localization of the FMR-1 gene product associated with fragile X syndrome

Characterization and localization of the FMR-1 gene product associated with fragile X syndrome

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_75797655

Characterization and localization of the FMR-1 gene product associated with fragile X syndrome

About this item

Full title

Characterization and localization of the FMR-1 gene product associated with fragile X syndrome

Publisher

London: Nature Publishing

Journal title

Nature (London), 1993-06, Vol.363 (6431), p.722-724

Language

English

Formats

Publication information

Publisher

London: Nature Publishing

More information

Scope and Contents

Contents

The fragile X syndrome is the most frequent form of inherited mental retardation after Down's syndrome, having an incidence of one in 1,250 males. The fragile X syndrome results from amplification of the CGG repeat found in the FMR-1 gene. This CGG repeat shows length variation in normal individuals and is increased significantly in both carriers a...

Alternative Titles

Full title

Characterization and localization of the FMR-1 gene product associated with fragile X syndrome

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_75797655

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_75797655

Other Identifiers

ISSN

0028-0836

E-ISSN

1476-4687

DOI

10.1038/363722a0

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