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Iterative Reanalysis of Hypertrophic Cardiomyopathy Exome Data Reveals Causative Pathogenic Mitochondrial DNA Variants.

Lopes, LR; Murphy, D; Bugiardini, E; Salem, R; Jager, J; Futema, M; Majid Akhtar, M; Savvatis, K; Woodward, C; Pittman, AM; et al. Lopes, LR; Murphy, D; Bugiardini, E; Salem, R; Jager, J; Futema, M; Majid Akhtar, M; Savvatis, K; Woodward, C; Pittman, AM; Hanna, MG; Syrris, P; Pitceathly, RDS; Elliott, PM (2021) Iterative Reanalysis of Hypertrophic Cardiomyopathy Exome Data Reveals Causative Pathogenic Mitochondrial DNA Variants. Circ Genom Precis Med, 14 (3). e003388. ISSN 2574-8300 https://doi.org/10.1161/CIRCGEN.121.003388
SGUL Authors: Futema, Marta Pittman, Alan Michael

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Item Type: Article
Additional Information: © 2021 The Authors. Circulation: Genomic and Precision Medicine is published on behalf of the American Heart Association, Inc., by Wolters Kluwer Health, Inc. This is an open access article under the terms of the Creative Commons Attribution Non-Commercial License, which permits use, distribution, and reproduction in any medium, provided that the original work is properly cited and is not used for commercial purposes.
Keywords: exome, genetics, hypertrophic cardiomyopathy, mitochondrial disease, exome, genetics, hypertrophic cardiomyopathy, mitochondrial disease
SGUL Research Institute / Research Centre: Academic Structure > Molecular and Clinical Sciences Research Institute (MCS)
Journal or Publication Title: Circ Genom Precis Med
ISSN: 2574-8300
Language: eng
Dates:
DateEvent
June 2021Published
10 May 2021Published Online
5 May 2021Accepted
Publisher License: Publisher's own licence
Projects:
Project IDFunderFunder ID
MR/S002065/1Medical Research Councilhttp://dx.doi.org/10.13039/501100000265
MR/S005021/1Medical Research Councilhttp://dx.doi.org/10.13039/501100000265
14 CVD03Fondation LeducqUNSPECIFIED
PubMed ID: 33970670
Web of Science ID: WOS:000661620500015
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/113278
Publisher's version: https://doi.org/10.1161/CIRCGEN.121.003388

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