@article{article, title  = {{Naturally occurring mineralocorticoid receptor mutations causing autosomal dominant pseudohypoaldosteronism type 1 (PHA1) - different pathogenetic molecular mechanisms resulting in diverse clinical phenotype}},

 url = {{}},

 year = {{2006}},

 month = {{1}},

 author = {{Riege FG and deSanctis L and Einaudi S and Testa A and Karges B and Sippell WG and Toth GF and Krone N}},

 volume = {{65}},

 journal = {{HORMONE RESEARCH}},

 pages = {{17-17}},

 note = {{Accessed on 2024/12/22}}}