Pseudohypoaldosteronism type 2: CUL3 mutation confirmed 15 years following initial diagnosis

Intern Med J. 2022 Apr;52(4):691-692. doi: 10.1111/imj.15740.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Cullin Proteins / genetics
  • Female
  • Humans
  • Mutation
  • Pseudohypoaldosteronism* / diagnosis
  • Pseudohypoaldosteronism* / genetics

Substances

  • CUL3 protein, human
  • Cullin Proteins