2a2fbd4b9e295fc244db623799ad1a9d pmc_33794951.pdf 47ec387ab617a6e281516245fcaf80bf3bf146b9 pmc_33794951.pdf 9c1429e47fd4c0789ed2963e62a6d2dccfb6b795f173b6e6ac5e127b7385f804 pmc_33794951.pdf Title: Correction to: Phenotypic characterization of X-linked hypophosphatemia in pediatric Spanish population Subject: Orphanet Journal of Rare Diseases, https://doi.org/10.1186/s13023-021-01786-5 Author: Enrique Rodríguez-Rubio Creator: Adobe InDesign 15.0 (Windows) Producer: Adobe PDF Library 15.0; modified using iText® 5.3.5 ©2000-2012 1T3XT BVBA (SPRINGER SBM; licensed version) CreationDate: Tue Mar 30 12:33:38 2021 CEST ModDate: Thu Apr 1 16:59:03 2021 CEST Tagged: no UserProperties: no Suspects: no Form: none JavaScript: no Pages: 1 Encrypted: no Page size: 595.276 x 790.866 pts Page rot: 0 File size: 574151 bytes Optimized: no PDF version: 1.4 name type encoding emb sub uni object ID ------------------------------------ ----------------- ---------------- --- --- --- --------- MyriadPro-Regular Type 1C Custom yes no yes 56 0 MyriadPro-Bold Type 1C WinAnsi yes no yes 57 0 MyriadPro-It Type 1C Custom yes no yes 58 0 WarnockPro-Regular Type 1C Custom yes no yes 59 0 MyriadPro-Light Type 1C Custom yes no yes 60 0 MyriadPro-Semibold Type 1C WinAnsi yes no yes 61 0 Jhove (Rel. 1.22.1, 2019-04-17) Date: 2021-09-11 03:35:20 CEST RepresentationInformation: pmc_33794951.pdf ReportingModule: PDF-hul, Rel. 1.12.1 (2019-04-17) LastModified: 2021-04-12 03:40:44 CEST Size: 574151 Format: PDF Version: 1.4 Status: Well-Formed and valid SignatureMatches: PDF-hul MIMEtype: application/pdf PDFMetadata: Objects: 119 FreeObjects: 1 IncrementalUpdates: 0 DocumentCatalog: ViewerPreferences: HideToolbar: false HideMenubar: false HideWindowUI: false FitWindow: false CenterWindow: false DisplayDocTitle: false NonFullScreenPageMode: UseNone Direction: L2R ViewArea: CropBox ViewClip: CropBox PrintArea: CropBox PageClip: CropBox PageLayout: SinglePage PageMode: UseOutlines Language: en-US Outlines: Item: Title: Correction to: Phenotypic characterization of X-linked hypophosphatemia in pediatric Spanish population Children: Item: Title: Correction to: Orphanet J Rare Dis (2021) 16:104 https:​doi.​org​10.​1186​s13023-​021–01729-0 Item: Title: References Info: Title: Correction to: Phenotypic characterization of X-linked hypophosphatemia in pediatric Spanish population Author: Enrique Rodríguez-Rubio Subject: Orphanet Journal of Rare Diseases, https://doi.org/10.1186/s13023-021-01786-5 Creator: Adobe InDesign 15.0 (Windows) Producer: Adobe PDF Library 15.0; 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If used as a dc:identifier, the URI form should be captured, and the bare identifier should also be captured using prism:doi. If an alternate unique identifier is used as the required dc:identifier, then the DOI should be specified as a bare identifier within prism:doi only. If the URL associated with a DOI is to be specified, then prism:url may be used in conjunction with prism:doi in order to provide the service endpoint (i.e. the URL). doi Text external ISSN for an electronic version of the issue in which the resource occurs. Permits publishers to include a second ISSN, identifying an electronic version of the issue in which the resource occurs (therefore e(lectronic)Issn. 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