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Authors: Peter, M Nikischin, W Heinz-Erian, P Fussenegger, W Kapelari, K Sippell, WG
Citation: M. Peter et al., Homozygous deletion of arginine-173 in the CYP11B2 gene in a girl with congenital hypoaldosteronism - Corticosterone methyloxidase deficiency type II, HORMONE RES, 50(4), 1998, pp. 222-225
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