[Congenital hypothyroidism. Molecular defects in familial disease]

Ann Endocrinol (Paris). 2003 Feb;64(1):54-7.
[Article in French]
No abstract available

Publication types

  • Review

MeSH terms

  • Animals
  • Congenital Hypothyroidism*
  • DNA-Binding Proteins / genetics
  • Forkhead Transcription Factors
  • Humans
  • Hypothyroidism / genetics*
  • Mice
  • Nuclear Proteins / genetics
  • PAX8 Transcription Factor
  • Paired Box Transcription Factors
  • Receptors, Thyrotropin / genetics
  • Repressor Proteins / genetics
  • Thyroid Gland / embryology
  • Thyroid Nuclear Factor 1
  • Trans-Activators / genetics
  • Transcription Factors / genetics

Substances

  • DNA-Binding Proteins
  • FOXE1 protein, human
  • Forkhead Transcription Factors
  • Nuclear Proteins
  • PAX8 Transcription Factor
  • PAX8 protein, human
  • Paired Box Transcription Factors
  • Pax8 protein, mouse
  • Receptors, Thyrotropin
  • Repressor Proteins
  • Thyroid Nuclear Factor 1
  • Trans-Activators
  • Transcription Factors