Kandari, S., Puri, R., Cheluvaiah, C., Biswal, A., Singh, A. and Ahlawat, P. (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), pp. 3911–3913. doi: 10.18203/2320-6012.ijrms20242661.