Computational and biophysical determination of pathogenicity of variants of unknown significance in cardiac thin filament
Author:
Funder
NIH-NHLBI
Publisher
American Society for Clinical Investigation
Subject
General Medicine
Link
https://insight.jci.org/articles/view/154350/files/pdf
Reference57 articles.
1. Cardiomyopathies
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3. A molecular basis for familial hypertrophic cardiomyopathy: A β cardiac myosin heavy chain gene missense mutation
4. Thin Filament Mutations
5. A systematic approach to assessing the clinical significance of genetic variants
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2. Basic science methods for the characterization of variants of uncertain significance in hypertrophic cardiomyopathy;Frontiers in Cardiovascular Medicine;2023-08-01
3. Molecular Dynamics Assessment of Mechanical Properties of the Thin Filaments in Cardiac Muscle;International Journal of Molecular Sciences;2023-03-01
4. Myofilament-associated proteins with intrinsic disorder (MAPIDs) and their resolution by computational modeling;Quarterly Reviews of Biophysics;2023
5. Thin filament cardiomyopathies: A review of genetics, disease mechanisms, and emerging therapeutics;Frontiers in Cardiovascular Medicine;2022-09-07
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