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The Capital Region of Denmark - a part of Copenhagen University Hospital
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Recessive Inheritance of a Rare Variant in the Nuclear Mitochondrial Gene for AARS2 in Late-Onset Dilated Cardiomyopathy

Research output: Contribution to journalLetterResearchpeer-review

  1. Genetic Determinants of Electrocardiographic P-Wave Duration and Relation to Atrial Fibrillation

    Research output: Contribution to journalJournal articleResearchpeer-review

  2. Randomization of Left-right Asymmetry and Congenital Heart Defects: The Role of DNAH5 in Humans and Mice

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  3. Subsequent Event Risk in Individuals With Established Coronary Heart Disease

    Research output: Contribution to journalJournal articleResearchpeer-review

  4. High-resolution Regulatory Maps Connect Vascular Risk Variants to Disease Related Pathways

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  5. Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR Interval

    Research output: Contribution to journalJournal articleResearchpeer-review

  1. Hemodynamic Determinants of Activity Measured by Accelerometer in Patients With Stable Heart Failure

    Research output: Contribution to journalJournal articleResearchpeer-review

  2. Left Ventricular Assist Devices at the Crossroad of Innovation in Advanced Heart Failure

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. Comprehensive Physiological Modeling Provides Novel Insights Into Heart Failure With Preserved Ejection Fraction Physiology

    Research output: Contribution to journalJournal articleResearchpeer-review

  4. A novel homoplasmic mt-tRNAGlu m.14701C>T variant presenting with a partially reversible infantile respiratory chain deficiency

    Research output: Contribution to journalJournal articleResearchpeer-review

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Original languageEnglish
Article numbere003086
JournalCirculation. Genomic and precision medicine
Volume13
Issue number5
Pages (from-to)560-562
Number of pages3
ISSN2574-8300
DOIs
Publication statusPublished - Oct 2020

    Research areas

  • cardiomyopathies, genes, heart failure, mitochondrial diseases, mutation, Heart failure, Genes, Cardiomyopathies, Mitochondrial diseases, Mutation

ID: 61437946