A novel PRKAR1A gene mutation associated with primary pigmented nodular adrenocortical disease

Am J Med Sci. 2014 Aug;348(2):177-8. doi: 10.1097/MAJ.0000000000000296.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Adrenal Cortex Diseases / genetics*
  • Child
  • Cyclic AMP-Dependent Protein Kinase RIalpha Subunit / genetics*
  • Female
  • Humans
  • Mutation*

Substances

  • Cyclic AMP-Dependent Protein Kinase RIalpha Subunit
  • PRKAR1A protein, human