Correction of renal tubular acidosis in carbonic anhydrase II-deficient mice with gene therapy.

Gelijkaardige items

• Renal tubular acidosis, osteopetrosis, and cerebral calcification: A rare syndrome caused by carbonic anhydrase II deficiency
  door: B A Laway, et al.
  Gepubliceerd in: (2017-01-01)
• Renal Tubular Acidosis, Osteopetrosis, and Cerebral Calcification: A Rare Syndrome Caused by Carbonic Anhydrase II Deficiency
  door: Laway, B. A., et al.
  Gepubliceerd in: (2017)
• Carbonic anhydrase II deficiency identified as the primary defect in the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcification.
  door: Sly, W S, et al.
  Gepubliceerd in: (1983)
• Inactive form of erythrocyte carbonic anhydrase B in patients with primary renal tubular acidosis.
  door: Kondo, T, et al.
  Gepubliceerd in: (1978)
• Enzymatically Inactive Red Cell Carbonic Anhydrase B in a Family with Renal Tubular Acidosis
  door: Shapira, Emmanuel, et al.
  Gepubliceerd in: (1974)