date: 2021-02-15T07:53:43Z pdf:PDFVersion: 1.7 pdf:docinfo:title: Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction xmp:CreatorTool: Elsevier access_permission:can_print_degraded: true subject: The American Journal of Human Genetics, 108 (2021) 346-356. doi:10.1016/j.ajhg.2021.01.007 language: en dc:format: application/pdf; version=1.7 pdf:docinfo:custom:robots: noindex pdf:docinfo:creator_tool: Elsevier access_permission:fill_in_form: true pdf:docinfo:custom:CreationDate--Text: 30th January 2021 pdf:encrypted: false dc:title: Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction modified: 2021-02-15T07:53:43Z cp:subject: The American Journal of Human Genetics, 108 (2021) 346-356. doi:10.1016/j.ajhg.2021.01.007 robots: noindex pdf:docinfo:custom:CrossMarkDomains[1]: sciencedirect.com pdf:docinfo:subject: The American Journal of Human Genetics, 108 (2021) 346-356. doi:10.1016/j.ajhg.2021.01.007 pdf:docinfo:creator: Joery den Hoed meta:author: Elke de Boer pdf:docinfo:custom:CrossmarkMajorVersionDate: 2010-04-23 access_permission:extract_for_accessibility: true pdf:docinfo:custom:CrossMarkDomains[2]: elsevier.com pdf:docinfo:custom:doi: 10.1016/j.ajhg.2021.01.007 ElsevierWebPDFSpecifications: 7.0 pdf:docinfo:custom:CrossmarkDomainExclusive: true Author: Elke de Boer producer: Acrobat Distiller 8.1.0 (Windows) CrossmarkDomainExclusive: true pdf:docinfo:producer: Acrobat Distiller 8.1.0 (Windows) doi: 10.1016/j.ajhg.2021.01.007 CreationDate--Text: 30th January 2021 pdf:unmappedUnicodeCharsPerPage: 1 dc:description: The American Journal of Human Genetics, 108 (2021) 346-356. doi:10.1016/j.ajhg.2021.01.007 access_permission:modify_annotations: true dc:creator: Elke de Boer description: The American Journal of Human Genetics, 108 (2021) 346-356. doi:10.1016/j.ajhg.2021.01.007 Last-Modified: 2021-02-15T07:53:43Z dcterms:modified: 2021-02-15T07:53:43Z title: Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction xmpMM:DocumentID: uuid:9b99e96b-c4ee-406a-8e7f-7582d36ffaf5 Last-Save-Date: 2021-02-15T07:53:43Z CrossMarkDomains[1]: sciencedirect.com pdf:docinfo:modified: 2021-02-15T07:53:43Z meta:save-date: 2021-02-15T07:53:43Z Content-Type: application/pdf X-Parsed-By: org.apache.tika.parser.DefaultParser creator: Elke de Boer dc:language: en pdf:docinfo:custom:ElsevierWebPDFSpecifications: 7.0 access_permission:assemble_document: true xmpTPg:NPages: 51 pdf:charsPerPage: 5613 access_permission:extract_content: true access_permission:can_print: true CrossMarkDomains[2]: elsevier.com access_permission:can_modify: true CrossmarkMajorVersionDate: 2010-04-23