Mutations in the chloride-bicarbonate exchanger gene AE1 cause autosomal dominant but not autosomal recessive distal renal tubular acidosis

Lignende værker

• Localization of a Gene for Autosomal Recessive Distal Renal Tubular Acidosis with Normal Hearing (rdRTA2) to 7q33-34
  af: Karet, Fiona E., et al.
  Udgivet: (1999)
• Molecular mechanisms of autosomal dominant and recessive distal renal tubular acidosis caused by SLC4A1 (AE1) mutations
  af: Yenchitsomanus, Pa-thai, et al.
  Udgivet: (2005)
• Novel ATP6V1B1 and ATP6V0A4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing loss
  af: Stover, E, et al.
  Udgivet: (2002)
• 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)
• Bicarbonate for acute acidosis
  af: Korang, Steven Kwasi, et al.
  Udgivet: (2021)