Smadar Cederboim-Horowitz
Jerusalem, JM, Israel
Last Updated: 09/26/2026
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Found 8 publications
Reconsidering a silent variant: SGCA's role in atypical cardiomyopathy.
Journal: European journal of human genetics : EJHG
Published: May 15, 2025
Missing in action: the genetic mysteries of extremely low HDL cholesterol.
Journal: Frontiers in cardiovascular medicine
Published: December 30, 2024
Calmodulinopathy Associated Long QT Syndrome, Hypertrophic Cardiomyopathy With Excessive Trabeculation in a 14-Year-Old Girl Presenting With Ventricular Fibrillation.
Journal: Circulation. Genomic and precision medicine
Published: January 23, 2024
Ser194Leu DSG2 mutation, associated with arrhythmogenic left ventricular cardiomyopathy and ventricular tachycardia.
Journal: Pacing and clinical electrophysiology : PACE
Published: August 27, 2023
Variable clinical expression of a novel FLNC truncating variant in a large family.
Journal: International journal of cardiology
Published: August 07, 2023
Acute Myocarditis Associated With Desmosomal Gene Variants.
Journal: JACC. Heart failure
Published: April 29, 2022
Homozygous stop-gain variant in LRRC32, encoding a TGFβ receptor, associated with cleft palate, proliferative retinopathy, and developmental delay.
Journal: European journal of human genetics : EJHG
Published: June 19, 2018
Showing 1-8 of 8
Last Updated: 09/26/2026