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Article

Neurobehavioural evidence for the involvement of the FMR1 gene in female carriers of fragile X syndrome.

Neuroscience and biobehavioral reviews - 1 Mar 2013

Kraan Claudine M, Hocking Darren R, Bradshaw John L, Fielding Joanne, Cohen Jonathan, Georgiou-Karistianis Nellie, Cornish Kim M

Abstract excerpt

For years, premutation-carriers of fragile X-syndrome (FXS) were assumed free from any deleterious phenotype. In this review, we discuss the current literature on neurocognitive, emotional and neuromotor profiles emerging in females with the fragile-X premutation, and discuss phenotypic profiles in male premutation-carriers to gain insights into possible underlying mechanisms associated with FMR1 gene expression....

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Source

Identifiers

PMID: 23352653
DOI: 10.1016/j.neubiorev.2013.01.010

Genes

FMR1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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