Genetic Polymorphisms that Playing Role in Development of Hypertrophic Cardiomyopathy
Author:
Alkanli Nevra,Ay Arzu
Reference16 articles.
1. Tirone AP, Arteaga E. Familial hypertrophic cardiomyopathy. Genetic characterization. Arquivos Brasileiros de Cardiologia. 1999;72(4):520-522
2. Iio C, Akiyoshi O, Nagai T, et al. Association between genetic variation in the SCN10A gene and cardiac conduction abnormalities in patients with hypertrophic cardiomyopathy. International Heart Journal. 2015;56:421-427
3. Manohar Rao PPK, Anjana M, Mullapudi R, et al. The M235T polymorphism of the angiotensinogen gene in South Indian patients of hypertrophic cardiomyopathy. Journal of the Renin-Angiotensin-Aldosterone System. 2010;12(3):238-242. DOI: 10.1177/1470320310387955
4. Güleç Ç, Abacı N, Bayrak F. Association between non-coding polymorphisms of HOPX gene and syncope in hypertrophic cardiomyopathy. Anadolu Kardiyoloji Dergisi. 2014;14:617-624. DOI: 10.5152/akd.2014.4972
5. Ji F, Liu Q, Feng Z, et al. Genetic association between 1425G/A SNP in PRKCH and hypertrophic cardiomyopathy in a Chinese population. Oncotarget. 2017;8(70):114839-114844