@article{927b019404fc4dddbedc65f3d067fa86,
title = "Spectrum of movement disorders and motor abnormalities in adults with a 22q11.2 microdeletion: Comment on the literature and retrospective study of 92 adults",
author = "Erik Boot and Connie Marras and Bassett, {Anne S}",
note = "Funding Information: The authors thank all participants and the families of the adults with 22q11.2DS for their participation, and Marcos Sanches (Krembil Centre for Neuroinformatics, CAMH) for review and critique of the statistical analysis. This work was supported financially by the Physicians{\textquoteright} Services Incorporated Foundation (15-15; to EB), the Canadian Institutes of Health Research (MOP 97800, MOP111238, PJT–169161 and PJT-148924; to ASB), and through donations from the W. Garfield Weston Foundation and Dalglish Family Foundation, the Dalglish Chair in 22q11.2 Deletion Syndrome at the University of Toronto and University Health Network (ASB), and the Dalglish Fellowship in 22q11.2 Deletion Syndrome (EB). Funding Information: The authors thank all participants and the families of the adults with 22q11.2DS for their participation, and Marcos Sanches (Krembil Centre for Neuroinformatics, CAMH) for review and critique of the statistical analysis. This work was supported financially by the Physicians{\textquoteright} Services Incorporated Foundation (15-15; to EB), the Canadian Institutes of Health Research (MOP 97800, MOP111238, PJT–169161 and PJT-148924; to ASB), and through donations from the W. Garfield Weston Foundation and Dalglish Family Foundation, the Dalglish Chair in 22q11.2 Deletion Syndrome at the University of Toronto and University Health Network (ASB), and the Dalglish Fellowship in 22q11.2 Deletion Syndrome (EB). ",
year = "2022",
month = dec,
doi = "10.1038/s41431-022-01152-4",
language = "English",
volume = "30",
pages = "1314--1317",
journal = "European Journal of Human Genetics",
issn = "1018-4813",
publisher = "Nature Publishing Group",
number = "12",
}