Molecular genetic study in two patients with congenital hypoaldosteronism (types I and II) in relation to previously published hormonal studies

1998-07-01

European Journal of Endocrinology , Volume 139 - Issue 1 p. 96- 100

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Persistent URL	doi.org/10.1530/eje.0.1390096, hdl.handle.net/1765/55805
Journal	European Journal of Endocrinology
Organisation	Department of Pediatrics
Citation APA Style AAA Style APA Style Cell Style Chicago Style Harvard Style IEEE Style MLA Style Nature Style Vancouver Style American-Institute-of-Physics Style Council-of-Science-Editors Style BibTex Format Endnote Format RIS Format CSL Format DOIs only Format	Peter, M., Bünger, K., Drop, S., & Sippell, W. (1998). Molecular genetic study in two patients with congenital hypoaldosteronism (types I and II) in relation to previously published hormonal studies. European Journal of Endocrinology, 139(1), 96–100. doi:10.1530/eje.0.1390096

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