Familial Glucocorticoid Deficiency: Advances in the Molecular Understanding of ACTH Action

No abstract is available for this paper.

• Publication year

  2007

• Venue

  Hormone Research in Paediatrics

• Publication date

  2007-12-05

• Fields of study

  Medicine

• Identifiers
  DOI 10.1159/000111810PMID 18059087
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Differential regulation of the human adrenocorticotropin receptor [melanocortin-2 receptor (MC2R)] by human MC2R accessory protein isoforms alpha and beta in isogenic human embryonic kidney 293 cells.

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• Severe loss-of-function mutations in the adrenocorticotropin receptor (ACTHR, MC2R) can be found in patients diagnosed with salt-losing adrenal hypoplasia

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