[HTML][HTML] Sarcomeric gene variants among Indians with hypertrophic cardiomyopathy: A scoping review

L Koshy, S Ganapathi, P Jeemon… - Indian Journal of …, 2023 - journals.lww.com
Hypertrophic cardiomyopathy (HCM) is a genetic heart muscle disease that frequently
causes sudden cardiac death (SCD) among young adults. Several pathogenic mutations in …

Association of South Asian-specific MYBPC3Δ25bp deletion polymorphism and cardiomyopathy: A systematic review and meta-analysis

L Koshy, P Jeemon, S Ganapathi, M Madhavan… - Meta Gene, 2021 - Elsevier
Background Inherited cardiomyopathies are a frequent cause of heart failure. A 25-basepair
deletion polymorphism MYBPC3 Δ25bp (rs36212066) in the MYBPC3 gene found …

Impact of the gene polymorphisms in the renin-angiotensin system on cardiomyopathy risk: A meta-analysis

X Jia, L Meng, W Tang, L Sun, F Peng, P Zhang - Plos one, 2024 - journals.plos.org
Due to the inconsistent findings from various studies, the role of gene polymorphisms in the
renin-angiotensin system in influencing the development of cardiomyopathy remains …