IGSF1 mutation as a cause of isolated central hypothyroidism

Endocrinol Diabetes Nutr (Engl Ed). 2022 Dec;69(10):913-914. doi: 10.1016/j.endien.2022.11.032. Epub 2022 Dec 1.
No abstract available

Publication types

  • Letter

MeSH terms

  • Congenital Hypothyroidism*
  • Humans
  • Immunoglobulins / genetics
  • Membrane Proteins / genetics
  • Mutation

Substances

  • IGSF1 protein, human
  • Immunoglobulins
  • Membrane Proteins