A neonatal form of isolated ACTH deficiency frequently associated with Tpit gene mutations

Endocr Res. 2004 Nov;30(4):943-4. doi: 10.1081/erc-200044166.
No abstract available

MeSH terms

  • Adrenocorticotropic Hormone / deficiency*
  • Genes, Recessive
  • Homeodomain Proteins / genetics*
  • Humans
  • Infant, Newborn
  • Mutation*
  • Steroid Metabolism, Inborn Errors / genetics*
  • T-Box Domain Proteins
  • Transcription Factors / genetics*

Substances

  • Homeodomain Proteins
  • T-Box Domain Proteins
  • TBX19 protein, human
  • Transcription Factors
  • Adrenocorticotropic Hormone