A novel TPM1 mutation in a family with hypertrophic cardiomyopathy and sudden cardiac death in childhood
Author:
Publisher
Elsevier BV
Subject
Cardiology and Cardiovascular Medicine
Reference16 articles.
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3. Australian National Genomic Information Service (ANGIS) Database. Available at FHC Mutation Database. Available at: http://www.angis.org.au/Databases/Heart/heartbreak.html. Accessed February 7, 2002
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1. In silico and in vitro models reveal the molecular mechanisms of hypocontractility caused by TPM1 M8R;Frontiers in Physiology;2024-08-30
2. Identification of a novel likely pathogenic TPM1 variant linked to hypertrophic cardiomyopathy in a family with sudden cardiac death;ESC Heart Failure;2024-06-14
3. Sudden Cardiac Death, Post-Mortem Investigation: A Proposing Panel of First Line and Second Line Genetic Tests;Journal of Personalized Medicine;2024-05-20
4. A Novel TPM1 Mutation Causes Familial Hypertrophic Cardiomyopathy in an Indian Family: Genetic and Clinical Correlation;Indian Journal of Clinical Biochemistry;2022-04-11
5. Genetic Clues on Implantable Cardioverter-Defibrillator Placement in Young-Age Hypertrophic Cardiomyopathy: A Case Report of Novel MYH7 Mutation and Literature Review;Frontiers in Cardiovascular Medicine;2021-12-23
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