ReviewBMC nephrology2018
A novel SLC12A3 homozygous c2039delG mutation in Gitelman syndrome with hypocalcemia.
Wenjun Yang et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.
5 papers cite it
this papercites it
ReviewBMC nephrology2018
Wenjun Yang et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.