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Case report
Open Access
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,
Autor para correspondencia
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

Artículo

This article is available in English

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

Wojciech Wolyniec, Sonia Kaniuka- Jakubowska, Mato Nagel, Zuzanna Wolyniec, Lukasz Obolonczyk, Renata Swiatkowska-Stodulska, Krzysztof Sworczak, Marcin Renke
10.1016/j.nefroe.2015.09.004
Nefrologia (English Version). 2016;36:304-9
Idiomas
Nefrología