Inactive form of erythrocyte carbonic anhydrase B in patients with primary renal tubular acidosis.

Lignende værker

• Enzymatically Inactive Red Cell Carbonic Anhydrase B in a Family with Renal Tubular Acidosis
  af: Shapira, Emmanuel, et al.
  Udgivet: (1974)
• Correction of renal tubular acidosis in carbonic anhydrase II-deficient mice with gene therapy.
  af: Lai, L W, et al.
  Udgivet: (1998)
• Carbonic anhydrase II deficiency identified as the primary defect in the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcification.
  af: Sly, W S, et al.
  Udgivet: (1983)
• Distal renal tubular acidosis in primary hyperparathyroidism
  af: Lo, Tom Edward Ngo, et al.
  Udgivet: (2015)
• Renal tubular acidosis, osteopetrosis, and cerebral calcification: A rare syndrome caused by carbonic anhydrase II deficiency
  af: B A Laway, et al.
  Udgivet: (2017-01-01)