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1. A homozygous DSC2 deletion associated with arrhythmogenic cardiomyopathy is caused by uniparental isodisomy. (April 2020)

2. Back Cover, Volume 40, Issue 6. Issue 6 (21st May 2019)

3. Cardiomyopathy‐associated mutations in the RS domain affect nuclear localization of RBM20. Issue 11 (9th September 2020)

5. Noncompaction cardiomyopathy is caused by a novel in‐frame desmin (DES) deletion mutation within the 1A coiled‐coil rod segment leading to a severe filament assembly defect. Issue 6 (3rd April 2019)

6. The emergency medical service has a crucial role to unravel the genetics of sudden cardiac arrest in young, out of hospital resuscitated patients: Interim data from the MAP-IT study. (November 2021)