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

Ngā tūemi rite

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