date: 2016-02-05T17:34:10Z pdf:PDFVersion: 1.3 pdf:docinfo:title: Characterisation of CASPR2 deficiency disorder - a syndrome involving autism, epilepsy and language impairment xmp:CreatorTool: Arbortext Advanced Print Publisher 9.1.440/W Unicode access_permission:can_print_degraded: true subject: BMC Medical Genetics, 2016, doi:10.1186/s12881-016-0272-8 pdfa:PDFVersion: A-2b xmpMM:History:Action: converted dc:format: application/pdf; version=1.3 pdf:docinfo:creator_tool: Arbortext Advanced Print Publisher 9.1.440/W Unicode access_permission:fill_in_form: true xmpMM:History:When: 2016-02-01T22:18:48Z pdf:encrypted: false dc:title: Characterisation of CASPR2 deficiency disorder - a syndrome involving autism, epilepsy and language impairment modified: 2016-02-05T17:34:10Z cp:subject: BMC Medical Genetics, 2016, doi:10.1186/s12881-016-0272-8 xmpMM:History:SoftwareAgent: pdfToolbox pdf:docinfo:custom:CrossMarkDomains[1]: springer.com pdf:docinfo:subject: BMC Medical Genetics, 2016, doi:10.1186/s12881-016-0272-8 xmpMM:History:InstanceID: uuid:0c3f349c-cd41-4971-85e0-bc0301979c40 pdf:docinfo:creator: Pedro Rodenas-Cuadrado meta:author: Nicola Pietrafusa meta:creation-date: 2016-02-01T14:07:50Z pdf:docinfo:custom:CrossmarkMajorVersionDate: 2016-02-01 created: 2016-02-01T14:07:50Z access_permission:extract_for_accessibility: true Creation-Date: 2016-02-01T14:07:50Z pdfaid:part: 2 pdf:docinfo:custom:CrossMarkDomains[2]: springerlink.com pdf:docinfo:custom:doi: 10.1186/s12881-016-0272-8 pdf:docinfo:custom:CrossmarkDomainExclusive: true Author: Nicola Pietrafusa producer: Acrobat Distiller 10.1.5 (Windows); modified using iText® 5.3.5 ©2000-2012 1T3XT BVBA (AGPL-version) CrossmarkDomainExclusive: true pdf:docinfo:producer: Acrobat Distiller 10.1.5 (Windows); modified using iText® 5.3.5 ©2000-2012 1T3XT BVBA (AGPL-version) doi: 10.1186/s12881-016-0272-8 pdf:unmappedUnicodeCharsPerPage: 0 dc:description: BMC Medical Genetics, 2016, doi:10.1186/s12881-016-0272-8 Keywords: CNTNAP2,Epilepsy,Intellectual disability,Language regression,Autism access_permission:modify_annotations: true dc:creator: Nicola Pietrafusa description: BMC Medical Genetics, 2016, doi:10.1186/s12881-016-0272-8 dcterms:created: 2016-02-01T14:07:50Z Last-Modified: 2016-02-05T17:34:10Z dcterms:modified: 2016-02-05T17:34:10Z title: Characterisation of CASPR2 deficiency disorder - a syndrome involving autism, epilepsy and language impairment xmpMM:DocumentID: uuid:3c99aa96-bc39-444c-8d12-280f7ead68d4 Last-Save-Date: 2016-02-05T17:34:10Z CrossMarkDomains[1]: springer.com pdf:docinfo:keywords: CNTNAP2,Epilepsy,Intellectual disability,Language regression,Autism pdf:docinfo:modified: 2016-02-05T17:34:10Z meta:save-date: 2016-02-05T17:34:10Z Content-Type: application/pdf X-Parsed-By: org.apache.tika.parser.DefaultParser creator: Nicola Pietrafusa pdfaid:conformance: B dc:subject: CNTNAP2,Epilepsy,Intellectual disability,Language regression,Autism access_permission:assemble_document: true xmpTPg:NPages: 7 pdf:charsPerPage: 3719 access_permission:extract_content: true access_permission:can_print: true CrossMarkDomains[2]: springerlink.com meta:keyword: CNTNAP2,Epilepsy,Intellectual disability,Language regression,Autism access_permission:can_modify: true pdf:docinfo:created: 2016-02-01T14:07:50Z CrossmarkMajorVersionDate: 2016-02-01