Orthophosphate transport in the erythrocyte of normal subjects and of patients with X-linked hypophosphatemia.

समान संसाधन

• The Gy mutation: another cause of X-linked hypophosphatemia in mouse.
  द्वारा: Lyon, M F, और अन्य
  प्रकाशित: (1986)
• Incorporation of orthophosphate-(32)P into erythrocyte phospholipids in normal subjects and in patients with hereditary spherocytosis
  द्वारा: Reed, Claude F.
  प्रकाशित: (1968)
• Primary cultures of renal epithelial cells from X-linked hypophosphatemic (Hyp) mice express defects in phosphate transport and vitamin D metabolism.
  द्वारा: Bell, C L, और अन्य
  प्रकाशित: (1988)
• X-linked hypophosphatemia: the mutant gene is expressed in teeth as well as in kidney.
  द्वारा: Shields, E D, और अन्य
  प्रकाशित: (1990)
• Hyperparathyroidism and Parathyroidectomy in X-linked Hypophosphatemia Patients
  द्वारा: DeLacey, Sean, और अन्य
  प्रकाशित: (2019)