1. Biondo, Elisa D, Spontarelli, Kerri, Ababioh, Giovanna, Méndez, Lois, Artigas, Pablo. 2021. Diseases caused by mutations in the Na+/K+ pump α1 gene ATP1A1. In American journal of physiology. Cell physiology, 321, C394-C408. doi:10.1152/ajpcell.00059.2021. https://pubmed.ncbi.nlm.nih.gov/34232746/
2. Gomez-Sanchez, Celso E, Kuppusamy, Maniselvan, Gomez-Sanchez, Elise P. 2014. Somatic mutations of the ATP1A1 gene and aldosterone-producing adenomas. In Molecular and cellular endocrinology, 408, 213-9. doi:10.1016/j.mce.2014.12.004. https://pubmed.ncbi.nlm.nih.gov/25496839/
3. Scholl, Ute I. 2022. Genetics of Primary Aldosteronism. In Hypertension (Dallas, Tex. : 1979), 79, 887-897. doi:10.1161/HYPERTENSIONAHA.121.16498. https://pubmed.ncbi.nlm.nih.gov/35139664/
4. Kashyap, Neeraj, Kumar, Pushpendra, Deshmukh, Bharti, Singh, Gyanendra, Sharma, Deepak. 2015. Association of ATP1A1 gene polymorphism with thermotolerance in Tharparkar and Vrindavani cattle. In Veterinary world, 8, 892-7. doi:10.14202/vetworld.2015.892-897. https://pubmed.ncbi.nlm.nih.gov/27047171/
5. Yuan, Yao, Yu, Lingqi, Zhuang, Xudong, Chen, Wenfeng, Wang, Xinrui. 2023. Drosophila models used to simulate human ATP1A1 gene mutations that cause Charcot-Marie-Tooth type 2 disease and refractory seizures. In Neural regeneration research, 20, 265-276. doi:10.4103/1673-5374.391302. https://pubmed.ncbi.nlm.nih.gov/38767491/
6. Megarbane, Andre, Bizzari, Sami, Deepthi, Asha, Delague, Valérie, Urtizberea, J Andoni. . A 20-year Clinical and Genetic Neuromuscular Cohort Analysis in Lebanon: An International Effort. In Journal of neuromuscular diseases, 9, 193-210. doi:10.3233/JND-210652. https://pubmed.ncbi.nlm.nih.gov/34602496/