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Article

Wild-type male offspring of fmr-1+/- mothers exhibit characteristics of the fragile X phenotype.

Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology - 1 Oct 2008

Zupan Bojana, Toth Miklos

Abstract excerpt

Fragile X syndrome is an X-linked disorder caused by the inactivation of the FMR-1 gene with symptoms ranging from impaired cognitive functions to seizures, anxiety, sensory abnormalities, and hyperactivity. Males are more severely affected than heterozygote (H) females, who, as carriers, have a...

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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: 18172434
DOI: 10.1038/sj.npp.1301651
PMCID: PMC2904748

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-18172434-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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