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
A second cohort of CHD3 patients expands the molecular mechanisms known to cause Snijders Blok-Campeau syndrome.
Drivas TG et al.
European Journal of Human Genetics : Ejhg, 2020
32483341 (PubMed )
Supplement: 41431_2020_654_MOESM1_ESM.xlsx › Table_S1
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