[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]
Authors
I Díez López
,
A Rodríguez Estevez
,
E González Molina
,
B Ezquieta Zubicaray
PMID:
19576599
DOI:
10.1016/j.medcli.2009.05.011
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