Brief report: congenital hyperthyroidism caused by a mutation in the thyrotropin-receptor gene

N Engl J Med. 1995 Jan 19;332(3):150-4. doi: 10.1056/NEJM199501193320304.
No abstract available

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Child
  • DNA Fingerprinting
  • Germ-Line Mutation*
  • Humans
  • Hyperthyroidism / congenital
  • Hyperthyroidism / genetics*
  • Infant, Newborn
  • Male
  • Molecular Sequence Data
  • Receptors, Thyrotropin / genetics*
  • Transfection

Substances

  • Receptors, Thyrotropin