SLC34A3 Intronic Deletion in an Iranian Kindred with Hereditary Hypophosphatemic Rickets with Hypercalciuria

Ítems similars

• SLC34A3 Intronic Deletion in a New Kindred with Hereditary Hypophosphatemic Rickets with Hypercalciuria
  per: Hasani-Ranjbar, Shirin, et al.
  Publicat: (2012)
• Intronic deletions in the SLC34A3 gene: A cautionary tale for mutation analysis of hereditary hypophosphatemic rickets with hypercalciuria
  per: Ichikawa, Shoji, et al.
  Publicat: (2013)
• HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA: A NOVEL HOMOZYGOUS MUTATION IN SLC34A3 AND LITERATURE REVIEW
  per: Bhadada, Sanjay K., et al.
  Publicat: (2020)
• Newly identified intronic and known pathogenic point mutations in SLC34A3/NPT2c cause hereditary hypophosphatemic rickets with hypercalciuria
  per: Yujing Sun, et al.
  Publicat: (2025-03-01)
• Hypophosphatemic Rickets with Hypercalciuria due to Mutation in SLC34A3/Type IIc Sodium-Phosphate Cotransporter: Presentation as Hypercalciuria and Nephrolithiasis
  per: Tencza, Amanda L., et al.
  Publicat: (2009)