1. Tanaka, M, Yamasaki, N, Izumo, S. . Phenotypic characterization of the murine Nkx2.6 homeobox gene by gene targeting. In Molecular and cellular biology, 20, 2874-9. doi:. https://pubmed.ncbi.nlm.nih.gov/10733590/
2. Ritter, Alyssa, Werner, Petra, Latney, Brande, Deardorff, Matthew A, Goldmuntz, Elizabeth. 2020. NKX2-6 related congenital heart disease: Biallelic homeodomain-disrupting variants and truncus arteriosus. In American journal of medical genetics. Part A, 182, 1454-1459. doi:10.1002/ajmg.a.61550. https://pubmed.ncbi.nlm.nih.gov/32198970/
3. Wang, Jun, Zhang, Dai-Fu, Sun, Yu-Min, Fang, Wei-Yi, Yang, Yi-Qing. 2014. NKX2-6 mutation predisposes to familial atrial fibrillation. In International journal of molecular medicine, 34, 1581-90. doi:10.3892/ijmm.2014.1971. https://pubmed.ncbi.nlm.nih.gov/25319568/
4. Wang, Juan, Mao, Jian-Hui, Ding, Ke-Ke, Xue, Song, Yang, Yi-Qing. 2014. A novel NKX2.6 mutation associated with congenital ventricular septal defect. In Pediatric cardiology, 36, 646-56. doi:10.1007/s00246-014-1060-x. https://pubmed.ncbi.nlm.nih.gov/25380965/
5. Zhao, Lan, Ni, Shi-Hong, Liu, Xing-Yuan, Yang, Yi-Qing, Qiu, Xing-Biao. 2014. Prevalence and spectrum of Nkx2.6 mutations in patients with congenital heart disease. In European journal of medical genetics, 57, 579-86. doi:10.1016/j.ejmg.2014.08.005. https://pubmed.ncbi.nlm.nih.gov/25195019/
6. Tanaka, M, Schinke, M, Liao, H S, Yamasaki, N, Izumo, S. . Nkx2.5 and Nkx2.6, homologs of Drosophila tinman, are required for development of the pharynx. In Molecular and cellular biology, 21, 4391-8. doi:. https://pubmed.ncbi.nlm.nih.gov/11390666/
智鼠故事 
