Two novel CYP21A2 missense mutations in Italian patients with 21-hydroxylase deficiency: Identification and functional characterisation.
IUBMB Life
; 61(3): 229-35, 2009 Mar.
Article
in En
| MEDLINE
| ID: mdl-19152428
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Type of study:
Diagnostic_studies
Language:
En
Journal:
IUBMB Life
Journal subject:
BIOLOGIA MOLECULAR
/
BIOQUIMICA
Year:
2009
Type:
Article
Affiliation country:
Italy