Novel compound heterozygous mutation of SLC12A3 in Gitelman syndrome co-existent with hyperthyroidism: A case report and literature review

por Qin, Yong-Zhang, Liu, Yan-Ming, Wang, Yang, You, Cong, Li, Long-Nian, Zhou, Xue-Yan, Lv, Wei-Min, Hong, Shi-Hua, Xiao, Li-Xia
Publicado 2022