Congenital hypothyroidism caused by a mutation in the Na+/l-symporter

Nat Genet. 1997 Sep;17(1):122. doi: 10.1038/ng0997-122a.
No abstract available

Publication types

  • Published Erratum

MeSH terms

  • Amino Acid Sequence
  • Base Sequence
  • Carrier Proteins / genetics*
  • Consensus Sequence
  • Humans
  • Hypothyroidism / genetics*
  • Introns
  • Membrane Proteins / genetics*
  • Molecular Sequence Data
  • Mutation*
  • Symporters*

Substances

  • Carrier Proteins
  • Membrane Proteins
  • Symporters
  • sodium-iodide symporter