A case report of Gitelman syndrome resulting from two novel mutations in SLC12A3 gene

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Case report

El caso del síndrome de Gitelman causado por dos nuevas mutaciones en el gen SLC12A3

Wojciech Wolynieca,

Corresponding author

wolyniecwojtek@gmail.com

Corresponding author.

, Sonia Kaniuka- Jakubowskab, Mato Nagelc, Zuzanna Wolyniecd, Lukasz Obolonczykb, Renata Swiatkowska-Stodulskab, Krzysztof Sworczakb, Marcin Renkea

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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Article information

ISSN: 20132514
Original language: English

DOI:10.1016/j.nefroe.2015.09.004

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2020 December	42	17	59
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