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Direction: L2R ViewArea: CropBox ViewClip: CropBox PrintArea: CropBox PageClip: CropBox PageLayout: SinglePage PageMode: UseOutlines Language: en-US Outlines: Item: Title: Homozygous R136S mutation in PRNP gene causes inherited early onset prion disease Children: Item: Title: Abstract Children: Item: Title: Background: Item: Title: Methods: Item: Title: Results: Item: Title: Conclusion: Item: Title: Background Item: Title: Materials and methods Children: Item: Title: Clinical data Item: Title: Genetic studies Item: Title: Neuropathology and immunoblotting Item: Title: In vitro propagation of PrP by PMCA Item: Title: Transmission studies in human PrP transgenic mice Item: Title: Western blotting in mouse bioassay Item: Title: Histological analysis in mouse bioassay Item: Title: Results Children: Item: Title: Clinical characterization and family history Item: Title: Genetic studies Item: Title: Neuropathological findings and immunoblotting Item: Title: In vitro propagation of PrPSc Item: Title: Bioassay in human-PrP transgenic mice Item: Title: Discussion Children: Item: Title: Limitations Item: Title: Conclusions Item: Title: Acknowledgements Item: Title: References Info: Title: Homozygous R136S mutation in Author: Teresa Ximelis Subject: Alzheimer's Research & Therapy, https://doi.org/10.1186/s13195-021-00912-6 Keywords: Gene;GSS;Homozygous;Neuropathology;Prion 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: Sat Oct 16 18:31:34 CEST 2021 ModDate: Mon Oct 18 14:01:56 CEST 2021 ID: 0x987f385566eb40a3ba8ed9193a6157b9, 0x35b9c014b54094423b92e4f7f18b3089 Filters: FilterPipeline: FlateDecode FilterPipeline: DCTDecode Images: Image: NisoImageMetadata: FormatName: image/png ImageWidth: 39 ImageHeight: 39 BitsPerSample: 8 BitsPerSampleUnit: integer Filter: FlateDecode Intent: RelativeColorimetric Decode: 0, 255 Name: X Image: NisoImageMetadata: FormatName: 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15.0; modified using iText® 5.3.5 ©2000-2012 1T3XT BVBA (SPRINGER SBM; licensed version) Gene;GSS;Homozygous;Neuropathology;Prion False application/pdf https://doi.org/10.1186/s13195-021-00912-6 BioMed Central Alzheimer's Research & Therapy, https://doi.org/10.1186/s13195-021-00912-6 Gene GSS Homozygous Neuropathology Prion Homozygous R136S mutation in Teresa Ximelis Alba Marín-Moreno Juan Carlos Espinosa Hasier Eraña Jorge M. 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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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