Journal of Biomedical Science is supported by the Ministry of Science and Technology (MOST), Taiwan.
A novel 9-bp insertion detected in steroid 21-hydroxylase gene (CYP21A2): prediction of its structural and functional implications by computational methods
Steroid 21-hydroxylase deficiency is the most common cause of congenital adrenal hyperplasia (CAH). Detection of underlying mutations in CYP21A2 gene encoding steroid 21-hydroxylase enzyme is helpful both for con...
Citation: Journal of Biomedical Science 2009 16:3