ARX, a novel Prd-class-homeobox gene highly expressed in the telencephalon, is mutated in X-linked mental retardation.
Hum Mol Genet
; 11(8): 981-91, 2002 Apr 15.
Article
en En
| MEDLINE
| ID: mdl-11971879
Investigation of a critical region for an X-linked mental retardation (XLMR) locus led us to identify a novel Aristaless related homeobox gene (ARX ). Inherited and de novo ARX mutations, including missense mutations and in frame duplications/insertions leading to expansions of polyalanine tracts in ARX, were found in nine familial and one sporadic case of MR. In contrast to other genes involved in XLMR, ARX expression is specific to the telencephalon and ventral thalamus. Notably there is an absence of expression in the cerebellum throughout development and also in adult. The absence of detectable brain malformations in patients suggests that ARX may have an essential role, in mature neurons, required for the development of cognitive abilities.
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Colección:
01-internacional
Asunto principal:
Telencéfalo
/
Factores de Transcripción
/
Genes Homeobox
/
Proteínas de Homeodominio
/
Cromosomas Humanos X
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Discapacidad Intelectual
/
Mutación
Límite:
Adolescent
/
Adult
/
Child
/
Child, preschool
/
Humans
/
Middle aged
Idioma:
En
Revista:
Hum mol genet
Asunto de la revista:
BIOLOGIA MOLECULAR
/
GENETICA MEDICA
Año:
2002
Tipo del documento:
Article
País de afiliación:
Francia