Castano, A. G.; de Nanclares, G. P.; Madariaga, L.; Aguirre, M.; Madrid, A.; Chocron, S.; Nadal, I.; Navarro, M.; Lucas, E.; Fijo, J.; Espino, M.; Espitaletta, Z.; Nieto, V. G.; de Frutos, D. B.; Loza, R.; Pintos, G.; Castano, L.; Ariceta, G.; RenalTube Group
(Public Library of Science, 2017)
Introduction: Type III Bartter syndrome (BS) is an autosomal recessive renal tubule disorder caused by loss-of-function mutations in the CLCNKB gene, which encodes the chloride channel protein ClC-Kb. In this study, we ...
