The authors of the article entitled, “Improved Diagnosis of Rare Disease Patients through Systematic Detection of Runs of Homozygosity” (Volume 22, pages 1205–1215 of the September 2020 issue of The Journal of Molecular Diagnostics; DOI: https://doi.org/10.1016/j.jmoldx.2020.06.008) have discovered an omission in the published Acknowledgments.
Additional Acknowledgement details: This research has been supported (not financially) by European Reference Network for rare malformation syndromes and rare intellectual and neurodevelopmental disorders, ERN-ITHACA (EU Framework Partnership Agreement ID: 3HP-HP-FPA ERN-01-2016/739516). This ERN is partly co-funded by the European Union within the framework of the Third Health Programme “ERN-2016—Framework Partnership Agreement 2017-2021.”