Systemic pseuhypodoaldosteronism type 1 caused by a novel mutation of SCNN1B gene: a case report and literature review

YANG Hanhua, WEN Lihua, XIE Lichun, et al

Journal of Clinical Pediatrics . 2019, (8): 605 - . DOI: 10.3969/j.issn.1000-3606.2019.08.012