Associated Papers
Mutations of ARX and non-syndromic intellectual disability in Chinese population.
Wu Y et al.
Genes & Genomics, 2019
Regulating transcriptional activity by phosphorylation: A new mechanism for the ARX homeodomain transcription factor.
Mattiske T et al.
Plos One, 2018
Expanding the phenotype associated with missense mutations of the ARX gene.
Charzewska A et al.
American Journal of Medical Genetics. Part A, 2013
ARX spectrum disorders: making inroads into the molecular pathology.
Shoubridge C et al.
Human Mutation, 2010
Screening of ARX in mental retardation families: Consequences for the strategy of molecular diagnosis.
Poirier K et al.
Neurogenetics, 2006
The role of ARX in cortical development.
Friocourt G et al.
The European Journal of Neuroscience, 2006
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