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A novel SLC12A3 homozygous c2039delG mutation in Gitelman syndrome with hypocalcemia

Wenjun Yang1, Shaoli Zhao1, Yanhong Xie1

  • 1The Endocrinology Department of the Third Xiangya Hospital, Central South University, Tongzipo Road, Changsha, 410013, China.

BMC Nephrology
|December 19, 2018
PubMed
Abstract

Keywords:
Gitelman syndromeHypocalcemiaSLC12A3 gene mutation

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