- Combined PTPN11 and MYBPC3 Gene Mutations in an Adult Patient with Noonan Syndrome and Hypertrophic Cardiomyopathy
Martina Caiazza et al, 2020, Genes CrossRef - Human Induced Pluripotent Stem Cell as a Disease Modeling and Drug Development Platform—A Cardiac Perspective
Mohamed M. Bekhite et al, 2021, Cells CrossRef - Proteomic profiling of sudden cardiac death with acquired cardiac hypertrophy
Yu Kakimoto et al, 2023, International Journal of Legal Medicine CrossRef - Genomic Insights into Cardiomyopathies: A Comparative Cross-Species Review
Siobhan Simpson et al, 2017, Veterinary Sciences CrossRef - Myocardial contractile proteins
Asim K. Duttaroy et al, 2024, Cellular, Molecular, and Environmental Contribution in Cardiac Remodeling CrossRef - Role of risk stratification and genetics in sudden cardiac death
Vikrant Rai et al, 2017, Canadian Journal of Physiology and Pharmacology CrossRef - Identification of a novel hypertrophic cardiomyopathy-associated mutation using targeted next-generation sequencing
Yue Zhao et al, 2017, International Journal of Molecular Medicine CrossRef - When Paying Attention Pays Back: Missense Mutation c.1006G>A p. (Val336Ile) in PRKAG2 Gene Causing Left Ventricular Hypertrophy and Conduction Abnormalities in a Caucasian Patient: Case Report and Literature Review
Emanuele Micaglio et al, 2024, International Journal of Molecular Sciences CrossRef - Pathogenicity of the Homoplasmic m.8701A>G Variant Requires Confirmation
Josef Finsterer et al, 2016, Chinese Medical Journal CrossRef - Massive Parallel DNA Sequencing of Patients with Inherited Cardiomyopathies in Cyprus and Suggestion of Digenic or Oligogenic Inheritance
Constantina Koutsofti et al, 2024, Genes CrossRef - Next Generation Sequencing Technologies
R. Rajesh Singh, 2017, Comprehensive Medicinal Chemistry III CrossRef