Family paralysis

Lancet. 2011 Jan 22;377(9762):352. doi: 10.1016/S0140-6736(10)61356-6.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Carrier State
  • Gitelman Syndrome / diagnosis*
  • Gitelman Syndrome / genetics*
  • Heterozygote
  • Humans
  • Male
  • Mutation
  • Paralysis / etiology*
  • Pedigree
  • Receptors, Drug / genetics
  • Reflex, Abnormal
  • Solute Carrier Family 12, Member 3
  • Symporters / genetics

Substances

  • Receptors, Drug
  • SLC12A3 protein, human
  • Solute Carrier Family 12, Member 3
  • Symporters