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

Podobne zapisy

• Mutations in the Chloride Channel Gene, CLCNKB, Leading to a Mixed Bartter-Gitelman Phenotype
  od: Nikola Jeck, i wsp.
  Wydane: (2000)
• Mutations in the Chloride Channel Gene CLCNKB as a Cause of Classic Bartter Syndrome
  od: Martin Konrad, i wsp.
  Wydane: (2000)
• A novel mutation of CLCNKB in a Korean patient of mixed phenotype of Bartter-Gitelman syndrome
  od: Cho, Hee-Won, i wsp.
  Wydane: (2016)
• Gitelman or Bartter type 3 syndrome? A case of distal convoluted tubulopathy caused by CLCNKB gene mutation
  od: Cruz, António José, i wsp.
  Wydane: (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, i wsp.
  Wydane: (2014)