1. Bagnall, Richard D, Singer, Emma S, Wacker, Julie, Weintraub, Robert G, Semsarian, Christopher. 2022. Genetic Basis of Childhood Cardiomyopathy. In Circulation. Genomic and precision medicine, 15, e003686. doi:10.1161/CIRCGEN.121.003686. https://pubmed.ncbi.nlm.nih.gov/36252119/
2. Jia, Lijuan, Chen, Yuanying, Hao, Chanjuan, Guo, Jun, Feng, Yingjun. . [Identification of variants in TNNI3 gene in two children with restrictive cardiomyopathy]. In Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics, 38, 731-734. doi:10.3760/cma.j.cn511374-20200602-00406. https://pubmed.ncbi.nlm.nih.gov/34365612/
3. Jordan, Elizabeth, Peterson, Laiken, Ai, Tomohiko, Ware, James, Hershberger, Ray E. 2021. Evidence-Based Assessment of Genes in Dilated Cardiomyopathy. In Circulation, 144, 7-19. doi:10.1161/CIRCULATIONAHA.120.053033. https://pubmed.ncbi.nlm.nih.gov/33947203/
4. Perrot, Andreas, Rickert-Sperling, Silke. . Human Genetics of Ventricular Septal Defect. In Advances in experimental medicine and biology, 1441, 505-534. doi:10.1007/978-3-031-44087-8_27. https://pubmed.ncbi.nlm.nih.gov/38884729/
5. Zhou, Nianwei, Weng, Haobo, Zhao, Weipeng, Pan, Cuizhen, Shu, Xianhong. . Gene-echocardiography: refining genotype-phenotype correlations in hypertrophic cardiomyopathy. In European heart journal. Cardiovascular Imaging, 25, 127-135. doi:10.1093/ehjci/jead200. https://pubmed.ncbi.nlm.nih.gov/37561025/