768b1f15bc89a20b6a08479de988cf51 pmc_9950119.pdf a8b72c51404b128b6831948dd4c643e8658a4429 pmc_9950119.pdf 9d08f4d83c5936cb975edb5a8ad16ad2d7060704b358e62ad5e9c6c3e4937d24 pmc_9950119.pdf Title: Molecular autopsy: Twenty years of post-mortem diagnosis in sudden cardiac death Subject: In the forensic medicine field, molecular autopsy is the post-mortem genetic analysis performed to attempt to unravel the cause of decease in cases remaining unexplained after a comprehensive forensic autopsy. Keywords: molecular autopsy, genetics, sudden cardiac death, inherited arrhythmogenic syndromes, forensic Author: Estefanía Martínez-Barrios Creator: LaTeX with hyperref package Producer: pdfTeX-1.40.16 CreationDate: Mon Feb 6 11:27:30 2023 CET ModDate: Mon Feb 6 12:21:27 2023 CET Tagged: no UserProperties: no Suspects: no Form: none JavaScript: no Pages: 12 Encrypted: no Page size: 595.276 x 841.89 pts (A4) Page rot: 0 File size: 2717596 bytes Optimized: no PDF version: 1.5 name type encoding emb sub uni object ID ------------------------------------ ----------------- ---------------- --- --- --- --------- LDVVHJ+MinionPro-Regular Type 1 Custom yes yes no 27 0 TWVABX+MuseoSans-700 Type 1 Custom yes yes no 28 0 LKQJBS+MuseoSans-300 Type 1 Custom yes yes no 29 0 XIZUJH+HelveticaNeueLTStd-Lt Type 1 Custom yes yes no 34 0 BVNLSU+MuseoSans-300Italic Type 1 Custom yes yes no 35 0 RLMHBQ+MuseoSans-500 Type 1 Custom yes yes no 36 0 UXIUNW+MinionPro-Bold Type 1 Custom yes yes no 112 0 XODHDR+RBLMI Type 1 Builtin yes yes no 116 0 DODMMZ+MinionPro-It Type 1 Custom yes yes no 117 0 CMERJW+MTGU Type 1 Builtin yes yes no 161 0 IPYESK+MTSYN Type 1 Builtin yes yes no 246 0 Jhove (Rel. 1.22.1, 2019-04-17) Date: 2023-07-12 02:30:36 CEST RepresentationInformation: pmc_9950119.pdf ReportingModule: PDF-hul, Rel. 1.12.1 (2019-04-17) LastModified: 2023-03-23 02:11:05 CET Size: 2717596 Format: PDF Version: 1.5 Status: Well-Formed and valid SignatureMatches: PDF-hul MIMEtype: application/pdf PDFMetadata: Objects: 816 FreeObjects: 2 IncrementalUpdates: 1 DocumentCatalog: PageLayout: SinglePage PageMode: UseOutlines Outlines: Item: Title: Molecular autopsy: Twenty years of post-mortem diagnosis in sudden cardiac death Children: Item: Title: 1. Introduction Item: Title: 2. Inherited arrhythmogenic syndromes Item: Title: 3. Channelopathies Children: Item: Title: 3.1. Long QT syndrome Item: Title: 3.2. Brugada syndrome Item: Title: 3.3. Short QT syndrome Item: Title: 3.4. Catecholaminergic polymorphic ventricular tachycardia Item: Title: 4. Cardiomyopathies Children: Item: Title: 4.1. Hypertrophic cardiomyopathy Item: Title: 4.2. Dilated cardiomyopathy Item: Title: 4.3. Arrhythmogenic cardiomyopathy Item: Title: 5. Genetic analysis/Interpretation Item: Title: 6. Samples Item: Title: 7. Recommendations/Guidelines Item: Title: 8. Medico-legal issues Item: Title: 9. Conclusion Item: Title: Author contributions Item: Title: Funding Item: Title: Conflict of interest Item: Title: Publisher's note Item: Title: References Info: Title: Molecular autopsy: Twenty years of post-mortem diagnosis in sudden cardiac death Author: Estefanía Martínez-Barrios Subject: In the forensic medicine field, molecular autopsy is the post-mortem genetic analysis performed to attempt to unravel the cause of decease in cases remaining unexplained after a comprehensive forensic autopsy. 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