Molecular Approach for Distal Renal Tubular Acidosis Associated AE1 Mutations

Ítems similars

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