SCNN1B基因突变致全身型假性醛固酮减少症1型1例报告并文献复习

杨汉华，温丽华，谢丽春，等

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

临床儿科杂志 . 2019, (8): 605 - . DOI: 10.3969/j.issn.1000-3606.2019.08.012