H62L Mutation of CYP21A2 Identified in the Non-classical Form of 21-Hydroxylase Deficiency
Clin Pediatr Endocrinol
.
2009 Oct;18(4):111-3.
doi: 10.1297/cpe.18.111.
Epub 2009 Nov 11.
Authors
Keisuke Nagasaki
1
,
Takeshi Usui
,
Tadashi Asami
,
Yohei Ogawa
,
Toru Kikuchi
,
Makoto Uchiyama
Affiliation
1
Division of Pediatrics, Department of Homeostatic Regulation and Development, Niigata University Graduate School of Medicine and Dental Sciences, Niigata, Japan.
PMID:
23926370
PMCID:
PMC3687609
DOI:
10.1297/cpe.18.111
No abstract available
Publication types
Case Reports