Clinical and Genetic Characterization of Patients with Bartter and Gitelman Syndrome

Bartter (BS) and Gitelman (GS) syndrome are autosomal recessive inherited tubulopathies, whose clinical diagnosis can be challenging, due to rarity and phenotypic overlap. Genotype–phenotype correlations have important implications in defining kidney and global outcomes. The aim of our study was to...

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Detalles Bibliográficos
Autores principales: Palazzo, Viviana, Raglianti, Valentina, Landini, Samuela, Cirillo, Luigi, Errichiello, Carmela, Buti, Elisa, Artuso, Rosangela, Tiberi, Lucia, Vergani, Debora, Dirupo, Elia, Romagnani, Paola, Mazzinghi, Benedetta, Becherucci, Francesca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9144947/
https://www.ncbi.nlm.nih.gov/pubmed/35628451
http://dx.doi.org/10.3390/ijms23105641

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9144947/
https://www.ncbi.nlm.nih.gov/pubmed/35628451
http://dx.doi.org/10.3390/ijms23105641

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