H.H. Lee
Kingcar Food Industrial Co.
Ltd., Yuan-Shan Research Institute
#86 Chen-Hsiang Road
China
Name/email consistency: high
- Multiple transcripts of the CYP21 gene are generated by the mutation of the splicing donor site in intron 2 from GT to AT in 21-hydroxylase deficiency. Lee, H.H., Chang, S.F. J. Endocrinol. (2001)
- Analysis of the chimeric CYP21P/CYP21 gene in steroid 21-hydroxylase deficiency. Lee, H.H., Chang, J.G., Tsai, C.H., Tsai, F.J., Chao, H.T., Chung, B. Clin. Chem. (2000)
- Use of TaqI digestion may lead to incorrect molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Lee, H.H., de Wijs, I.J., Sistermans, E.A. Mol. Genet. Metab. (2000)