DOI:
10.1055/s-00000025
Hormone and Metabolic Research
LinksClose Window
References
Choi JH, Jin HY, Ko JM, Lee JJ, Kim GH, Jung CW, Lee J, Yoo HW.
Clinical phenotype and mutation spectrum of the CYP21A2 gene in patients with steroid 21-hydroxylase deficiency.
Exp Clin Endocrinol Diabetes 2012;
120: 23-27
Search in:
Access:
We do not assume any responsibility for the contents of the web pages of other providers.