{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["35(7)"],"submitter":["Cunningham AC"],"funding":["Medical Research Council Canada","MRF","Medical Research Foundation","Medical Research Council","NIMH NIH HHS","National Institute of Mental Health","Health and Care Research Wales","Wellcome Trust","Waterloo Foundation"],"journal":["Movement disorders : official journal of the Movement Disorder Society"],"pagination":["1272-1274"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC7516340"],"repository":["biostudies-literature"],"pubmed_title":["Movement Disorder Phenotypes in Children With 22q11.2 Deletion Syndrome."],"pmcid":["PMC7516340"],"funding_grant_id":["MRC Post‐Doctoral Clinical Research Fellowship awarded to THM","G0801418","U01 MH101724","G0800509","5UO1MH101724","MR/L011166/1","MR/N022572/1","MR/P001629/1","MRF-154-0001-RG-SKUSE","503147","Early Career Research Fellowship awarded to ACC","507556","MR/T033045/1","MR/P008593/1","MR/L010305/1","MRF_MRF-154-0001-RG-SKUSE","918‐1234"],"pubmed_authors":["Owen MJ","Massey TH","Hall J","Fung W","Cunningham AC","van den Bree MBM","Peall KJ"],"additional_accession":[]},"is_claimable":false,"name":"Movement Disorder Phenotypes in Children With 22q11.2 Deletion Syndrome.","description":null,"dates":{"release":"2020-01-01T00:00:00Z","publication":"2020 Jul","modification":"2025-04-04T01:08:39.354Z","creation":"2025-04-04T01:08:39.354Z"},"accession":"S-EPMC7516340","cross_references":{"pubmed":["32379361"],"doi":["10.1002/mds.28078"]}}