Absence epilepsy and the CHD2 gene: an adolescent male with moderate intellectual disability, short-lasting psychoses, and an interstitial deletion in 15q26.1–q26.2

Overview of attention for article published in Neuropsychiatric Disease and Treatment, May 2016

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So far, Dimensions has found 13 publications that cite this research output.

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The most recent citing publications are shown below. View all 13 publications that cite this research output on Dimensions.

Chapter 5 CHROMO domain readers: A rainbow of opportunities

Book chapter (January 2024)

A novel de novo frameshift variant in the CHD2 gene related to intellectual and developmental disability, seizures and speech problems

Article in Molecular Genetics & Genomic Medicine (October 2023)

Clinical analysis of CHD2 gene mutations in pediatric patients with epilepsy

Article in Pediatric Investigation (April 2022)