Gitelman syndrome - A new mutation in the SLC12A3 gene

Nefrologia (Engl Ed). 2022 Jul-Aug;42(4):490-492. doi: 10.1016/j.nefroe.2022.06.002.

Authors

Ana Luísa Correia¹, Maria Guedes Marques², Rui Alves³

Affiliations

¹ Nephrology Department, Centro Hospitalar e Universitário de Coimbra EPE, Coimbra, Portugal. Electronic address: analuisadcorreia@gmail.com.
² Nephrology Department, Centro Hospitalar e Universitário de Coimbra EPE, Coimbra, Portugal.
³ Nephrology Department, Centro Hospitalar e Universitário de Coimbra EPE, Coimbra, Portugal; Nephrology Universitary Clinic, Universidade de Coimbra Faculdade de Medicina, Coimbra, Portugal.

PMID: 36460433
DOI: 10.1016/j.nefroe.2022.06.002

No abstract available

Publication types

Letter

MeSH terms

Gitelman Syndrome* / genetics
Humans
Mutation
Solute Carrier Family 12, Member 3 / genetics

Substances

SLC12A3 protein, human
Solute Carrier Family 12, Member 3