Autosomal Dominant PKD in Patients With PKD2 Mutations-A Benign Disorder?

Am J Kidney Dis. 2017 Oct;70(4):456-457. doi: 10.1053/j.ajkd.2017.06.009.
No abstract available

Publication types

  • Editorial
  • Comment

MeSH terms

  • Humans
  • Mutation
  • Polycystic Kidney, Autosomal Dominant*
  • Prevalence
  • Prognosis
  • TRPP Cation Channels / genetics

Substances

  • TRPP Cation Channels