Hereditary Hypophosphatemic Rickets with Hypercalciuria Is Caused by Mutations in the Sodium-Phosphate Cotransporter Gene SLC34A3

Lignende værker

• Loss-of-Function ENPP1 Mutations Cause Both Generalized Arterial Calcification of Infancy and Autosomal-Recessive Hypophosphatemic Rickets
  af: Lorenz-Depiereux, Bettina, et al.
  Udgivet: (2010)
• Hypophosphatemic Rickets with Hypercalciuria due to Mutation in SLC34A3/Type IIc Sodium-Phosphate Cotransporter: Presentation as Hypercalciuria and Nephrolithiasis
  af: Tencza, Amanda L., et al.
  Udgivet: (2009)
• Variable Clinical Presentation of Children With Hereditary Hypophosphatemic Rickets With Hypercalciuria: A Case Series
  af: Christensen, Stephanie, et al.
  Udgivet: (2021)
• HYPOPHOSPHATEMIC RICKETS
  af: N. N. Kartamysheva, et al.
  Udgivet: (2013-07-01)
• Hypophosphatemic rickets
  af: Jagtap, Varsha S., et al.
  Udgivet: (2012)