TY - JOUR
T1 - Correction
T2 - Clinical findings and a DNA methylation signature in kindreds with alterations in ZNF711 (European Journal of Human Genetics, (2022), 30, 4, (420-427), 10.1038/s41431-021-01018-1)
AU - Wang, Jiyong
AU - Foroutan, Aidin
AU - Richardson, Ellen
AU - Skinner, Steven A.
AU - Reilly, Jack
AU - Kerkhof, Jennifer
AU - Curry, Cynthia J.
AU - Tarpey, Patrick S.
AU - Robertson, Stephen P.
AU - Maystadt, Isabelle
AU - Keren, Boris
AU - Dixon, Joanne W.
AU - Skinner, Cindy
AU - Stapleton, Rachel
AU - Ruaud, Lyse
AU - Gumus, Evren
AU - Lakeman, Phillis
AU - Alders, Mariëlle
AU - Tedder, Matthew L.
AU - Schwartz, Charles E.
AU - Friez, Michael J.
AU - Sadikovic, Bekim
AU - Stevenson, Roger E.
PY - 2023
Y1 - 2023
N2 - Correction to: European Journal of Human Genetics, 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. The original article has been corrected.
AB - Correction to: European Journal of Human Genetics, 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. The original article has been corrected.
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85178482395&origin=inward
UR - https://www.ncbi.nlm.nih.gov/pubmed/38040915
U2 - 10.1038/s41431-023-01499-2
DO - 10.1038/s41431-023-01499-2
M3 - Erratum/Corrigendum
C2 - 38040915
SN - 1018-4813
JO - European journal of human genetics
JF - European journal of human genetics
ER -