Last Updated: 09/26/2026
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Found 102 publications
Damaging RBM20 E-rich domain variants are not rescued by gene replacement.
Journal: bioRxiv : the preprint server for biology
Published: July 29, 2026
Variant Site-Specific Natural History of Titin-Induced Cardiomyopathy: An International Multicenter Registry.
Journal: Circulation. Genomic and precision medicine
Published: July 08, 2026
Correction to: The Natural History of Massive Left Ventricular Hypertrophy in Pediatric Hypertrophic Cardiomyopathy: A Multiregistry Analysis.
Journal: Circulation
Published: June 22, 2026
Novel Truncating Variant c.1222DupC in RBM20 Causes Cardiomyopathy Consistent With Haploinsufficiency.
Journal: Circulation. Genomic and precision medicine
Published: April 30, 2026
RBM20 Truncating Variants and Human Cardiomyopathy.
Journal: JAMA cardiology
Published: April 08, 2026
Truncating Variants in TTN are Associated With Primary Atrial Myopathy.
Journal: Journal of the American Heart Association
Published: March 10, 2026
Leveraging the shared and opposing genetic mechanisms in the heritable cardiomyopathies.
Journal: Research square
Published: February 06, 2026
Generation of two induced pluripotent stem cell lines from female patients harboring MYH7 mutations with hypertrophic cardiomyopathy.
Journal: Stem cell research
Published: February 04, 2026
Last Updated: 09/26/2026