No evidence for coding region mutations in the retinoblastoma-associated Kruppel-associated box protein gene (RBaK) causing familial hyperaldosteronism type II

Clin Endocrinol (Oxf). 2006 Dec;65(6):829-31. doi: 10.1111/j.1365-2265.2006.02674.x.
No abstract available

Publication types

  • Letter

MeSH terms

  • Adult
  • Chromosomes, Human, Pair 7 / genetics
  • DNA Mutational Analysis
  • Female
  • Humans
  • Hyperaldosteronism / genetics*
  • Kruppel-Like Transcription Factors / genetics*
  • Male
  • Middle Aged
  • Mutation*
  • Open Reading Frames / genetics*
  • Retinoblastoma Protein / genetics*

Substances

  • Kruppel-Like Transcription Factors
  • Retinoblastoma Protein