Case report
A case report of Gitelman syndrome resulting from two novel mutations in SLC12A3 gene
El caso del síndrome de Gitelman causado por dos nuevas mutaciones en el gen SLC12A3
Wojciech Wolynieca,
, Sonia Kaniuka- Jakubowskab, Mato Nagelc, Zuzanna Wolyniecd, Lukasz Obolonczykb, Renata Swiatkowska-Stodulskab, Krzysztof Sworczakb, Marcin Renkea
Corresponding author
a Department of Occupational and Internal Medicine, Institute of Maritime and Tropical Medicine, Medical University of Gdansk, Poland
b Department of Endocrinology and Internal Medicine, Medical University of Gdansk, Poland
c Center for Nephrology and Metabolic Disorders, Weisswasser, Germany
d Department of Nephrology, Transplantology and Internal Medicine, Medical University of Gdansk, Poland
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