Published May 26, 2023
| Version v1
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Etges et al. "A novel homozygous KLHL3 mutation as a cause of autosomal recessive pseudohypoaldosteronism type II diagnosed late in life"
Authors/Creators
- 1. Department of Nephrology, School of Medicine, Heinrich-Heine-Universität Düsseldorf, Universitätsstraße 1, 40225 Düsseldorf, Germany
- 2. Charité – Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Department of Nephrology and Medical Intensive Care, Charitéplatz 1, 10117 Berlin, Germany
- 3. DaVita Dialysezentrum Dormagen, Elsa-Brändström-Str. 17, 41540 Dormagen, Germany
- 4. Berlin Institute of Health at Charité – Universitätsmedizin Berlin, Center of Functional Genomics, Charitéplatz 1, 10117 Berlin, Germany
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Raw data for Etges et al. "A novel homozygous KLHL3 mutation as a cause of autosomal recessive pseudohypoaldosteronism type II diagnosed late in life"
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