[De novo I172N mutation in a patient with 21-hydroxilase deficiency]

Med Clin (Barc). 2010 Jul 3;135(4):189-91. doi: 10.1016/j.medcli.2009.05.011. Epub 2009 Jul 2.
[Article in Spanish]
No abstract available

Publication types

  • Case Reports
  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenal Hyperplasia, Congenital / genetics*
  • Female
  • Humans
  • Infant, Newborn
  • Mutation*
  • Pedigree