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Article

Mouse models of fragile X-related disorders.

Disease models & mechanisms - 1 Feb 2023

Willemsen Rob, Kooy R Frank

Abstract excerpt

The fragile X-related disorders are an important group of hereditary disorders that are caused by expanded CGG repeats in the 5' untranslated region of the FMR1 gene or by mutations in the coding sequence of this gene. Two categories of pathological CGG repeats are associated with these disorders, full mutation alleles and shorter premutation alleles. Individuals with full mutation alleles develop fragile X...

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Share to Fragile X Mental Retardation Protein
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 36692473
DOI: 10.1242/dmm.049485
PMCID: PMC9903145

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

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