Associated Papers
Predicting the Damaging Potential of Uncharacterized KCNQ1 and KCNE1 Variants.
Tarnovskaya SI et al.
International Journal of Molecular Sciences, 2025
40724807 (PubMed )
Supplement: ijms-26-06561-s001.zip › ijms-3705358_SupplementaryTable1.xlsx › SupplementaryTable1_upd
Morphological and Genetic Aspects for Post-Mortem Diagnosis of Hypertrophic Cardiomyopathy: A Systematic Review.
Cianci V et al.
International Journal of Molecular Sciences, 2024
Loperamide Toxicity Revealing Apical Hypertrophic Cardiomyopathy.
Khan N et al.
Methodist Debakey Cardiovascular Journal, 2021
HPO-driven virtual gene panel: a new efficient approach in molecular autopsy of sudden unexplained death.
Schön U et al.
Bmc Medical Genomics, 2021
Mutations of Voltage-Gated Ionic Channels and Risk of Severe Cardiac Arrhythmias.
Dehghani-Samani A et al.
Acta Cardiologica Sinica, 2019
Role of genetic polymorphisms of ion channels in the pathophysiology of coronary microvascular dysfunction and ischemic heart disease.
Fedele F et al.
Basic Research in Cardiology, 2013
Mutations in the Kv1.5 channel gene KCNA5 in cardiac arrest patients.
Nielsen NH et al.
Biochemical and Biophysical Research Communications, 2007
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