Familial hyperkalemic hypertension: phenotypic analysis in a large family with the WNK1 deletion mutation

Am J Med. 2003 Apr 15;114(6):495-8. doi: 10.1016/s0002-9343(03)00054-8.
No abstract available

MeSH terms

  • Adolescent
  • Adult
  • Child
  • Gene Deletion*
  • Humans
  • Hyperkalemia / genetics*
  • Hypertension / genetics*
  • Intracellular Signaling Peptides and Proteins
  • Introns
  • Middle Aged
  • Minor Histocompatibility Antigens
  • Pedigree
  • Phenotype
  • Protein-Serine-Threonine Kinases / genetics*
  • Pseudohypoaldosteronism / genetics*
  • Syndrome
  • WNK Lysine-Deficient Protein Kinase 1

Substances

  • Intracellular Signaling Peptides and Proteins
  • Minor Histocompatibility Antigens
  • Protein-Serine-Threonine Kinases
  • WNK Lysine-Deficient Protein Kinase 1
  • WNK1 protein, human