DOI:
10.1055/s-00000025
Hormone and Metabolic Research
LinksClose Window
References
Muhammad E, Leventhal N, Parvari G, Hanukoglu A, Hanukoglu I, Chalifa-Caspi V, Feinstein Y, Weinbrand J, Jacoby H, Manor E, Nagar T, Beck JC, Sheffield VC, Hershkovitz E, Parvari R.
Autosomal recessive hyponatremia due to isolated salt wasting in sweat associated with a mutation in the active site of carbonic anhydrase 12.
Hum Genet 2011;
129: 397-340
We do not assume any responsibility for the contents of the web pages of other providers.