Correction to: European Journal of Human Genetics https://doi.org/10.1038/s41431-021-01018-1, published online 7 January 2022
The Data availability statement was incorrect and should have read as follows.
The summarized, anonymized data for each subject in this study are described in the text. Publicly available DNA methylation datasets have been deposited in GEO, and include data referring to various developmental syndromes (e.g., Kabuki syndrome, Sotos syndrome, CHARGE syndrome, immunodeficiency-centromeric instability-facial anomalies (ICF) syndrome, Williams-Beuren syndrome, Chr7q11.23 duplication syndrome, BAFopathies, Down syndrome), a large cohort of unresolved subjects with developmental delay/intellectual disability and congenital abnormalities, and also several large cohorts of DNA methylation data from the general population. Data in the EpiSign Knowledge Database, including methylation data from this ZNF711 study cohort, are not available due to Research Ethics Board and institutional restrictions. EpiSignTM is proprietary software and is not publicly available.
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Wang, J., Foroutan, A., Richardson, E. et al. Correction: Clinical findings and a DNA methylation signature in kindreds with alterations in ZNF711. Eur J Hum Genet (2023). https://doi.org/10.1038/s41431-023-01499-2
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DOI: https://doi.org/10.1038/s41431-023-01499-2
