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A genetic defect resulting in mild low-renin hypertension.

A genetic defect resulting in mild low-renin hypertension. Proc Natl Acad Sci U S A. 1998 Aug 18; 95(17):10200-5.

View in: PubMed

subject areas
  • 11-beta-Hydroxysteroid Dehydrogenases
  • Adolescent
  • Base Sequence
  • Child
  • Child, Preschool
  • Consanguinity
  • Cortisone
  • DNA Mutational Analysis
  • DNA Primers
  • Female
  • Homozygote
  • Humans
  • Hydrocortisone
  • Hydroxysteroid Dehydrogenases
  • Hypertension
  • Infant
  • Male
  • Metabolism, Inborn Errors
  • Mineralocorticoids
  • Pedigree
  • Point Mutation
  • Renin

authors with profiles
  • Robert C Wilson