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. International Journal of Research in Medical Sciences, [S. l.], v. 12, n. 10, p. 3911–3913, 2024. DOI: 10.18203/2320-6012.ijrms20242661. Disponível em: https://www.msjonline.org/index.php/ijrms/article/view/14078. Acesso em: 13 nov. 2025.