Original investigationProtein-coding mutations in the transcription factor-encoding gene ARX cause various forms of intellectual disability (ID) and epilepsy. In contrast, variations in surrounding non-coding sequences are correlated with milder forms of non-syndromic ID and autism and had suggested the importance of ARX gene regulation in the etiology of these disorders. We compile data on several novel and some already identified patients with or without ID that carry duplications of ARX genomic region and consider likely genetic mechanisms underlying the neurodevelopmental defects. We establish the long-range regulatory domain of ARX and identify its brain region-specific autoregulation. We conclude that neurodevelopmental disturbances i...
Intellectual disability (ID) and epilepsy often occur together and have a dramatic impact on the dev...
International audienceIntellectual disability (ID) and epilepsy often occur together and have a dram...
The production and integration of GABAergic interneurons into the cortex is a crucial element of bra...
The X-linked gene encoding aristaless-related homeobox (ARX) is a bi-functional transcription factor...
Mutations in the aristaless-related homeobox (ARX) gene are associated with multiple neurologic diso...
The Aristaless-related homeobox (ARX) gene encodes a paired-type homeodomain transcription factor wi...
Intellectual disability (ID) affects ~1-3% of the population, profoundly impacting the lives of affe...
The Aristaless-related homeobox gene (ARX, OMIM# 300382)located in chromosome Xp21.3 belongs to a fa...
Item does not contain fulltextPURPOSE: We describe a novel neurobehavioral phenotype of autism spect...
Item does not contain fulltextInvestigation of a critical region for an X-linked mental retardation ...
Intellectual disability (ID) and epilepsy often occur together and have a dramatic impact on the dev...
Intellectual disability (ID) and epilepsy often occur together and have a dramatic impact on the dev...
The Aristaless-related homeobox gene (ARX) is one of the most frequently mutated genes in a spectrum...
International audienceMutations in the Aristaless related homeobox (ARX) gene are associated with a ...
Intellectual disability (ID) and epilepsy often occur together and have a dramatic impact on the dev...
International audienceIntellectual disability (ID) and epilepsy often occur together and have a dram...
The production and integration of GABAergic interneurons into the cortex is a crucial element of bra...
The X-linked gene encoding aristaless-related homeobox (ARX) is a bi-functional transcription factor...
Mutations in the aristaless-related homeobox (ARX) gene are associated with multiple neurologic diso...
The Aristaless-related homeobox (ARX) gene encodes a paired-type homeodomain transcription factor wi...
Intellectual disability (ID) affects ~1-3% of the population, profoundly impacting the lives of affe...
The Aristaless-related homeobox gene (ARX, OMIM# 300382)located in chromosome Xp21.3 belongs to a fa...
Item does not contain fulltextPURPOSE: We describe a novel neurobehavioral phenotype of autism spect...
Item does not contain fulltextInvestigation of a critical region for an X-linked mental retardation ...
Intellectual disability (ID) and epilepsy often occur together and have a dramatic impact on the dev...
Intellectual disability (ID) and epilepsy often occur together and have a dramatic impact on the dev...
The Aristaless-related homeobox gene (ARX) is one of the most frequently mutated genes in a spectrum...
International audienceMutations in the Aristaless related homeobox (ARX) gene are associated with a ...
Intellectual disability (ID) and epilepsy often occur together and have a dramatic impact on the dev...
International audienceIntellectual disability (ID) and epilepsy often occur together and have a dram...
The production and integration of GABAergic interneurons into the cortex is a crucial element of bra...