Evolutionary dissection of mtDNA hg H: a susceptibility factor for hypertrophic cardiomyopathy-Reference-Cited by-同舟云学术

Evolutionary dissection of mtDNA hg H: a susceptibility factor for hypertrophic cardiomyopathy

Published:2020-06-30 Issue:6 Volume:31 Page:238-244
ISSN:2470-1394
Container-title:Mitochondrial DNA Part A
language:en
Short-container-title:Mitochondrial DNA Part A

Author:

Hagen Christian M.¹²,Elson Joanna L.¹³,Hedley Paula L.¹,Aidt Frederik H.¹,Havndrup Ole⁴,Jensen Morten K.⁵,Kanters Jørgen K.²,Atherton John J.⁶,McGaughran Julie⁷,Bundgaard Henning⁵,Christiansen Michael¹²

Affiliation:

1. Department for Congenital Disorders, Statens Serum Institute, Copenhagen, Denmark

2. Department of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark

3. Biosciences Institute, Newcastle University, Newcastle upon Tyne, UK

4. Department of Cardiology, Roskilde Hospital, Roskilde, Denmark

5. Department of Medicine B, The Heart Center, Copenhagen, Denmark

6. Department of Cardiology, Royal Brisbane Hospital and School of Medicine, University of Queensland, Brisbane, Australia

7. Queensland Clinical Genetics Service, Royal Children’s Hospital and School of Medicine, Brisbane, Australia

Publisher

Informa UK Limited

Subject

Genetics,Molecular Biology

Link

https://www.tandfonline.com/doi/pdf/10.1080/24701394.2020.1782897

Reference56 articles.

1. Genetic and phenotypic characterization of mutations in myosin-binding protein C (MYBPC3) in 81 families with familial hypertrophic cardiomyopathy: total or partial haploinsufficiency

2. Diagnostic yield, interpretation, and clinical utility of mutation screening of sarcomere encoding genes in Danish hypertrophic cardiomyopathy patients and relatives

3. A Novel Myosin Essential Light Chain Mutation Causes Hypertrophic Cardiomyopathy with Late Onset and Low Expressivity

4. Cardiac involvement in mitochondrial DNA disease: clinical spectrum, diagnosis, and management

5. Bybjerg-Grauholm J, Hagen CM, Goncalves VF, Baekvad-Hansen M, Hansen CS, Hedley PL, Kanters JK, Nielsen J, Theisen M, Mors O, Kennedy , et al. 2017. Mitochondrial DNA SNPs associated with schizophrenia exbibit highly variable inter-allelic haplogroup affiliation and nuclear genogeographic affinity bi-genomic linkage disequilibrium raises major concerns for link to disease. doi: https://doi.org/10.1101/149070. https://www.biorxiv.org/content/10.1101/149070v1

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