Associated Papers
In vivo base editing of Chd3 rescues behavioural abnormalities in mice.
Yang K et al.
Nature, 2026
Two distinct phenotypes in Snijders Blok-Campeau syndrome and characterization of the behavioral phenotype in a zebrafish model.
Enomoto Y et al.
European Journal of Human Genetics : Ejhg, 2025
Insights From a Novel Splicing Variant and Recurrent Arginine Variants in the CHD3 Gene Causing Snijders Blok-Campeau Syndrome.
Tie X et al.
American Journal of Medical Genetics. Part A, 2025
Snijders Blok-Campeau Syndrome: Description of 20 Additional Individuals with Variants in CHD3 and Literature Review.
Pascual P et al.
Genes, 2023
Genetic Variability of the Functional Domains of Chromodomains Helicase DNA-Binding (CHD) Proteins.
Cardoso AR et al.
Genes, 2021
A set of regulatory genes co-expressed in embryonic human brain is implicated in disrupted speech development.
Eising E et al.
Molecular Psychiatry, 2019
CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.
Snijders Blok L et al.
Nature Communications, 2018
Select a paper to view details