Poor phenotype-genotype association in a large series of patients with Type III Bartter syndrome

INTRODUCTION: Type III Bartter syndrome (BS) is an autosomal recessive renal tubule disorder caused by loss-of-function mutations in the CLCNKB gene, which encodes the chloride channel protein ClC-Kb. In this study, we carried out a complete clinical and genetic characterization in a cohort of 30 pa...

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Detalles Bibliográficos
Autores principales: García Castaño, Alejandro, Pérez de Nanclares, Gustavo, Madariaga, Leire, Aguirre, Mireia, Madrid, Álvaro, Chocrón, Sara, Nadal, Inmaculada, Navarro, Mercedes, Lucas, Elena, Fijo, Julia, Espino, Mar, Espitaletta, Zilac, García Nieto, Víctor, Barajas de Frutos, David, Loza, Reyner, Pintos, Guillem, Castaño, Luis, Ariceta, Gema
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5348002/
https://www.ncbi.nlm.nih.gov/pubmed/28288174
http://dx.doi.org/10.1371/journal.pone.0173581

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5348002/
https://www.ncbi.nlm.nih.gov/pubmed/28288174
http://dx.doi.org/10.1371/journal.pone.0173581

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