A novel mutation in the chloride channel gene, CLCNKB, as a cause of Gitelman and Bartter syndromes

Samankaltaisia teoksia

• Mutations in the Chloride Channel Gene, CLCNKB, Leading to a Mixed Bartter-Gitelman Phenotype
  Tekijä: Nikola Jeck, et al.
  Julkaistu: (2000)
• Mutations in the Chloride Channel Gene CLCNKB as a Cause of Classic Bartter Syndrome
  Tekijä: Martin Konrad, et al.
  Julkaistu: (2000)
• A novel mutation of CLCNKB in a Korean patient of mixed phenotype of Bartter-Gitelman syndrome
  Tekijä: Cho, Hee-Won, et al.
  Julkaistu: (2016)
• Gitelman or Bartter type 3 syndrome? A case of distal convoluted tubulopathy caused by CLCNKB gene mutation
  Tekijä: Cruz, António José, et al.
  Julkaistu: (2013)
• Mixed Bartter-Gitelman syndrome: an inbred family with a heterogeneous phenotype expression of a novel variant in the CLCNKB gene
  Tekijä: Al-Shibli, Amar, et al.
  Julkaistu: (2014)