Kandari, S., Puri, R., Cheluvaiah, C., Biswal, A., Singh, A., & 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), 3911–3913. https://doi.org/10.18203/2320-6012.ijrms20242661