Novel human pathological mutations. Gene symbol: PKD1. Disease: human autosomal dominant polycystic kidney disease

Hum Genet. 2007 Nov;122(3-4):413-4.
No abstract available

MeSH terms

  • Amino Acid Substitution
  • Codon / genetics
  • Codon, Nonsense
  • Humans
  • Polycystic Kidney, Autosomal Dominant / genetics*
  • TRPP Cation Channels*

Substances

  • Codon
  • Codon, Nonsense
  • TRPP Cation Channels
  • polycystic kidney disease 1 protein