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Article

A phenotypic and molecular characterization of the fmr1-tm1Cgr fragile X mouse.

Genes, brain, and behavior - 1 Dec 2004

Yan Q J, Asafo-Adjei P K, Arnold H M, Brown R E, Bauchwitz R P

Abstract excerpt

Fragile X Syndrome is the most common form of inherited mental retardation. It is also known for having a substantial behavioral morbidity, including autistic features. In humans, Fragile X Syndrome is almost always caused by inactivation of the X-linked FMR1 gene. A single knockout mouse model, fmr1-tm1Cgr, exists. In this report we further characterize the cognitive and behavioral phenotype of the fmr1-tm1Cgr...

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Source

Identifiers

PMID: 15544577
DOI: 10.1111/j.1601-183X.2004.00087.x

Genes

FMR1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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