A novel mutation in the chloride channel gene, CLCNKB, as a cause of Gitelman and Bartter syndromes
Shranjeno v:
Main Authors: | Israel Zelikovic, Raymonde Szargel, Ali Hawash, Valentina Labay, Ihab Hatib, Nadine Cohen, Farid Nakhoul |
---|---|
Format: | Artigo |
Jezik: | angleščina |
Izdano: |
2003
|
Online dostop: | https://doi.org/10.1046/j.1523-1755.2003.00730.x |
Oznake: |
Označite
Brez oznak, prvi označite!
|
Podobne knjige/članki
-
Mutations in the Chloride Channel Gene, CLCNKB, Leading to a Mixed Bartter-Gitelman Phenotype
od: Nikola Jeck, et al.
Izdano: (2000) -
Mutations in the Chloride Channel Gene CLCNKB as a Cause of Classic Bartter Syndrome
od: Martin Konrad, et al.
Izdano: (2000) -
A novel mutation of CLCNKB in a Korean patient of mixed phenotype of Bartter-Gitelman syndrome
od: Cho, Hee-Won, et al.
Izdano: (2016) -
Gitelman or Bartter type 3 syndrome? A case of distal convoluted tubulopathy caused by CLCNKB gene mutation
od: Cruz, António José, et al.
Izdano: (2013) -
Mixed Bartter-Gitelman syndrome: an inbred family with a heterogeneous phenotype expression of a novel variant in the CLCNKB gene
od: Al-Shibli, Amar, et al.
Izdano: (2014)