Molecular Approach for Distal Renal Tubular Acidosis Associated AE1 Mutations

Lignende værker

• Molecular mechanisms of autosomal dominant and recessive distal renal tubular acidosis caused by SLC4A1 (AE1) mutations
  af: Yenchitsomanus, Pa-thai, et al.
  Udgivet: (2005)
• Familial distal renal tubular acidosis is associated with mutations in the red cell anion exchanger (Band 3, AE1) gene.
  af: Bruce, L J, et al.
  Udgivet: (1997)
• Novel AE1 mutations in recessive distal renal tubular acidosis. Loss-of-function is rescued by glycophorin A.
  af: Tanphaichitr, V S, et al.
  Udgivet: (1998)
• Molecular Investigation of Distal Renal Tubular Acidosis in Tunisia, Evidence for Founder Mutations
  af: Nagara, Majdi, et al.
  Udgivet: (2014)
• Mutations in the chloride-bicarbonate exchanger gene AE1 cause autosomal dominant but not autosomal recessive distal renal tubular acidosis
  af: Karet, F. E., et al.
  Udgivet: (1998)