Genetic disorders of renal phosphate transport

N Engl J Med. 2010 Oct 28;363(18):1774; author reply 1774-5. doi: 10.1056/NEJMc1008407.
No abstract available

Publication types

  • Letter
  • Comment

MeSH terms

  • Abnormalities, Multiple / genetics
  • Histone Methyltransferases
  • Histone-Lysine N-Methyltransferase
  • Humans
  • Hypophosphatemia / genetics*
  • Intracellular Signaling Peptides and Proteins / genetics
  • Kidney / metabolism*
  • Male
  • Metabolism, Inborn Errors / genetics*
  • Mutation
  • Nuclear Proteins / genetics
  • Phosphates / metabolism*
  • Sodium-Phosphate Cotransporter Proteins, Type IIa / genetics*
  • Syndrome

Substances

  • Intracellular Signaling Peptides and Proteins
  • Nuclear Proteins
  • Phosphates
  • SLC34A1 protein, human
  • Sodium-Phosphate Cotransporter Proteins, Type IIa
  • Histone Methyltransferases
  • Histone-Lysine N-Methyltransferase
  • NSD1 protein, human