Kandari, Sharon, Rohit Puri, Chandrashekar Cheluvaiah, Anshuman Biswal, Arshdeep Singh, and Parul Ahlawat. 2024. “Bartter’s Syndrome Type II Due to a Novel Mutation in KCNJ1 Gene Presenting in Adulthood As Recurrent Hypokalaemic Periodic Paralysis”. International Journal of Research in Medical Sciences 12 (10):3911-13. https://doi.org/10.18203/2320-6012.ijrms20242661.