Understanding the molecular basis of cardiomyopathy
ML Bang, J Bogomolovas… - American Journal of …, 2022 - journals.physiology.org
Inherited cardiomyopathies are a major cause of mortality and morbidity worldwide and can
be caused by mutations in a wide range of proteins located in different cellular …
be caused by mutations in a wide range of proteins located in different cellular …
Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathy
Clinical presentation of congenital heart disease is heterogeneous, making identification of
the disease-causing genes and their genetic pathways and mechanisms of action …
the disease-causing genes and their genetic pathways and mechanisms of action …
[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 …
causes sudden cardiac death (SCD) among young adults. Several pathogenic mutations in …
Novel MYBPC3 Mutations in Indian Population with Cardiomyopathies
DS Rani, A Kasala, PS Dhandapany… - Pharmacogenomics …, 2023 - Taylor & Francis
Background Mutations in Myosin Binding Protein C (MYBPC3) are one of the most frequent
causes of cardiomyopathies in the world, but not much data are available in India. Methods …
causes of cardiomyopathies in the world, but not much data are available in India. Methods …
Novel variations in β-myosin heavy-chain gene (β-MYH7) and its association in south Indian women with cardiomyopathies
Background Mutations in β-MYH7 gene is a main genetic cause of cardiomyopathy and
sudden cardiac arrest, yet the molecular mechanisms have not been fully understood …
sudden cardiac arrest, yet the molecular mechanisms have not been fully understood …