Congenital hypothyroidism caused by mutations in the thyrotropin-receptor gene

N Engl J Med. 1997 May 8;336(19):1390-1. doi: 10.1056/NEJM199705083361914.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Congenital Hypothyroidism*
  • Germ-Line Mutation*
  • Humans
  • Hypothyroidism / genetics*
  • Infant, Newborn
  • Receptors, Thyrotropin / genetics*
  • Thyroid Gland / pathology

Substances

  • Receptors, Thyrotropin