(1)
Kandari, S.; Puri, R.; Cheluvaiah, C.; Biswal, A.; Singh, A.; Ahlawat, P. Bartter’s Syndrome Type II Due to a Novel Mutation in KCNJ1 Gene Presenting in Adulthood As Recurrent Hypokalaemic Periodic Paralysis. Int J Res Med Sci 2024, 12, 3911-3913.